• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Racemic or optionally active 2-(propargyloxyimino)-1,7,7-trimethyl-bicyclo[2,2,1]heptane of the formula (I) <IMAGE> (I) or a mixture of these isomers is prepared by reacting a racemic or optically active 1,7,7-trimethyl-bicyclo[2,2,1]heptane derivative of the general formula (II), <IMAGE> (II) wherein Y stands for oxygen atom, sulfur atom or oxime group, with a propyne derivative of the general formula (III), R-CH2-C 3BOND CH (III) wherein R stands for halogen atom or aminooxy group, with the proviso that if Y represents oxime group, R may stand only for halogen, and if R represents aminooxy group, Y may stand only for oxygen or sulfur atom.
    公开号:SU1248532A3
    申请号:SU843803960
    申请日:1984-10-19
    公开日:1986-07-30
    发明作者:Будаи Золтан；Юрак Ференц；Киш-Тамаш Аттила；Лаи Аранка；Мезей Тибор；Виг Золтан；Зубовитш Терез
    申请人:Эдьт Дьедьсерведьесети Дьяр (Инопредприятие)；
    IPC主号:
    专利说明:

      . 12D8532J.
    The invention relates to a method for the cycle of (2, 2, 1) -he-11-tane in the form of spot-emission of a new 2- (propargyloxy-imino) -, 7,7-trimethylbicyclo- (2.2.1) - heptane of formula
    yellow oil. T. KNP. 94-96 ° C; 1.5 mmHg ; Hjj ° 1, D953.
    Example 3. 39, Og (0.1 mol) of finely divided sodium amide is added to 800 ml of xylene and treated with a solution of 167 g (0, .1 mol) (i) -1, 7, 7 of trimethylbicyclic (2, 2.1) heptan-2-one-oxime in 200 ml of dimethylformamide. After completion of the formation of gas at the same temperature, 74.5 g (1.0 mol) of propargyl chloride was added to the reaction mixture. After 2 h, the reaction mixture is washed
    N-0 CH2-CsCH
    in the form of the racemate and / or in the optically active form, which can be used as plant growth regulators, at the same time possessing insecticidal properties.
    The aim of the invention is to develop Example 3. 39, Og (0.1 mol) of fine-grained sodium amide is added to 800 ml of xylene and treated with a solution of 167 g (0, .1 mol) (i) -1, 7, 7 trimethylbicyclo (2,2,1) -heptan-2-one-oxime in 200 ml of dimethylformamide. After completion of the formation of gas at the same temperature, 74.5 g (1.0 mol) of propargyl chloride was added to the reaction mixture. After 2 h, the reaction mixture is washed.
    20
    25
    Development of a new method for producing water. The content of the biologically active substance in the xylene phase is determined by microtiterm.
    812 kg of a xylene solution containing 23.8% of (+) -2-pro-pargyloxyimino-1,7,7-trimethylbicyclo (2, 2, l) -heptane are obtained, yield 94.2%.
    Example 4. To a solution of 76, g (0.5 mol) (i) -, 7,7-trimethylbicyc-. Lo (2,2,) - heptan-2-one in 225 ml of pyridine and 450 ml of anhydrous ethanol was added 59.0 g (0.55 ml) of propargyloxyimine hydrochloride. The reaction mixture is boiled for 3 hours and then evaporated under vacuum. The remainder. treated with water and the product is extracted with dichloroethane. The organic phase is evaporated and the residue is fractionated under vacuum,
    Obtain 76.0 g (74.0%) (±) -2- (pro 35 pargiloxyimino) -, 7,7-trimethylbicyclo (2, 2, 1) -heptane in the form of a light yellow oil .. T.p.92 WITH; 1.0mm Hg
    waterborne in r d. bicyclo (2, 2,1) teptane with high activity as plant growth regulators,
    Example 1: 4.6 g (0.2 mol) of metallic sodium was dissolved in 200 ml of methanol. To the solution was added 33.4 g (0.2 mol) (±) - 1.7.7- trimethylbicyclo (2,2,1) -heptan-2-on-oxime. The mixture is boiled for 1 hour and then 23.8 g (0.2 mol) of propargyl bromide are processed, after 1 hour the reaction time is cooled, The sodium bromide precipitated is filtered off, the filtrate is filtered in and the residue is fractionated under vacuum.
    33.2 g (81%) of (t) 2-pro-pargilloxyimino-1,7,7-trimethylbicyclo (2.2.1) -heptane are obtained in the form of a light yellow oil. T, kip,.
    thirty
    1.5 mm Hg, with t,
    m
     1.4955,
    Calculated,%: C 76.05; H 9.33; N 6.82, C, jH N O
    Found,%: C 76.17; H 9.62; N 6.88,
    Example 2, 4.8 g (0.2 mol) of sodium hydride was added to 150 ml of anhydrous benzene. At 50 ° C, a solution of 33.4 g (0.2 mol) of (t) -1, 7, 7-trimethylbitseIllo (2.2, 1) -heptan-2-one-oxime in 50 ml is added over half an hour dimethylformamide. After the gas has formed, the mixture is cooled to and treated with 23.8 g (0.2 mol) of propargyl bromide. After 2 h, the reaction mixture is washed with water, the organic phase is separated, embedded and the residue is fractionated under vacuum.
    37.0 g are obtained (90.5% (+} -2 - propargyloxyimino-1,7,7-trimethylbi G
     1.4956.
    40
    Example 5. The method is carried out according to example 4, however, it comes out of 76.0 g (0.5 mol) of (-) -1,7,7-tri-,. methylbicyclo (2,2,1) -heptan-2-one.
    79.0 g (77.9%) of (-) -2- 45 - (propargyloxyimino) -1.7,7-trimethyl-bicyclo (2.2.1) -heptane are obtained. Bp 94 ° C;
    1.5 mmHg ; P
    ten
     J, 4955;
    50
    S5
    .-20.02 ± 1 ° vC 1, methanol).
    Example 6. The method is carried out according to Example 4, however, it comes from 84.0 g (0.5 mol) - (t) -1, 7,7-trimethylbicyclo (2.2.1) -hep-. tan-2-tion. 81.0 g (79%) of (+) -2-propargyloxyimino -1,7,7-trimethylbicyclo (2.2.1) -heptane are obtained. Bp 92 C; 1.0 mmHg, PE 1.4956; cclJJ +20,08 ± 1 ° (C 1, methanol).
    yellow oil. T. KNP. 94-96 ° C; 1.5 mmHg ; Hjj ° 1, D953.
    Example 3. 39, Og (0.1 mol) of finely divided sodium amide is added to 800 ml of xylene and treated with a solution of 167 g (0, .1 mol) (i) -1, 7, 7 of trimethylbicyclic (2, 2.1) heptan-2-one-oxime in 200 ml of dimethylformamide. After completion of the formation of gas at the same temperature, 74.5 g (1.0 mol) of propargyl chloride was added to the reaction mixture. After 2 h, the reaction mixture is washed.
    water The content of the biologically active substance in the xylene phase is determined by microtiterm.
    Get 76 argiloksiimin about (2, 2, 1) -hepple of that oil .. T
     R
     1.4956.
    Example 5. The method is carried out according to example 4, however, it comes out of 76.0 g (0.5 mol) of (-) -1,7,7-tri-,. methylbicyclo (2,2,1) -heptan-2-one.
    79.0 g (77.9%) of (-) -2- - (propargyloxyimino) -1,7,7-trimethyl-bicyclo (2.2.1) -heptane are obtained. Bp 94 ° C;
    1.5 mmHg ; P
    ten
     J, 4955;
    .-20.02 ± 1 ° vC 1, methanol).
    Example 6. The method is carried out according to Example 4, however, it comes from 84.0 g (0.5 mol) - (t) -1, 7,7-trimethylbicyclo (2.2.1) -hep-. tan-2-tion. 81.0 g (79%) of (+) -2-propargyloxyimino -1,7,7-trimethylbicyclo (2.2.1) -heptane are obtained. Bp 92 C; 1.0 mmHg, PE 1.4956; cclJJ +20,08 ± 1 ° (C 1, methanol).
    Example 7, 40.0 g (1.0 mol) of micronized NaOH and 50 ml of methanol are introduced into 800 ml of xylene. The mixture is boiled for 30 minutes with stirring, then cooled to 30 ° C and treated with 167.0 g (1.0 mol) of (+) -1,7,7- - trimethylbicyclo (2.2.1) -heptane 2-on-oxime. The reaction mixture is again slowly brought to a boil, methyl alcohol is distilled off through a Markuson nozzle and 18 ml (1.0 mol) of water formed during the reaction. After distillation of water, the reaction mixture is cooled to 30 ° C and then treated with 200 ml of anhydrous dimethylformamide, then, with cooling, 119.0 g (1.0 mol) of propargyl bromide are treated at the same temperature. The mixture was allowed to react for 2 hours at 30 ° C and then washed several times with water. The organic phase is dried over calcined magnesium sulphate, the content of the active substance is determined by microtitling. 835.0 g of a solution containing 23.7% (+) 2- (propargyloxy-imino) -1,7,7-trimethylbicyclo (2.2.1) - heptane is obtained. The yield is 96.5%.
    Untreated control
    Coating without biologically active substance
    Biologically active coating
    From Table 1 it can be seen that there is no difference between the untreated control and the grains covered with a non-biologically active substance within the permissible error, while plants grown from
    0
    five
    0
    Example 8. The test of growth stimulation, a) Experiments in the greenhouse.
     In the seedling pot filled with sand, 3x30 maize kernels were planted, in each case 10 grains were left untreated, 10 grains were treated according to example 10 with Placebo etching agent that does not contain biologically active material (10 more With a biologically active substance containing an etching agent, the pots were placed in a greenhouse with optimum temperature and humidity conditions for maize. The number of germinated grains was calculated in percent. On the 14th and 28th day after sowing, divided the height and green mass of the plants. The germination rate was determined as a percentage, and the height and green mass were correlated with the corresponding reference value (100).
    The results are presented in Table 1.
    Table 1
    100 100 100 SHO
    105 102 103 99
    143,152,148,154
    grains treated with a biologically active substance were 43-48% higher and 52-54% more green mass than both controls (untreated and Placebo - processed).
     $ 12
    With “,) | In seedling pots sized 20x20 cm filled with sand and placed in a greenhouse, they planted beans, carrots, flax, paprika 3 tomatoes, barley, millet, and spent post-harvest treatment with a biologically active substance according to the proposed method with a dose of 0.1 kg racemate - biologically active substance / ha or 0.2 kg of the racemate biologically active substance / ha. AT . at 4 weeks of age, the green mass of the plants was determined and compared to untreated control plants.
    The results are presented in table 2.
    table 2


    Green mass of plants,%, treated with biologically active substance dose, kg / ha
    From Table 2 it can be seen that plant crops such as flax, tomatoes, spinach and barley, treated with a biologically active substance with a dose of 0.1 kg / ha, have achieved more favorable results, while for the rest of the crops, a more favorable dose is 0 , 2 kg / ha. The increase in green mass compared to non-inverse control is 18-40%.
    f Experiments on small cases in free ground.
    The experiment with seed dressing, described under b), was repeated on
    Lnke size 1 m, however, take into account the general vegetation periods. The harvested corn cobs were weighed, weeds were destroyed by weeding.
    The results are presented in table 3. Table 3
    0
    five
    0
    Untreated control
    Coating without biologically active substance
    Biologically active coating
    100 100
    100
    98
    103
    101
    127 125
    120
    From Table 3, it can be seen that corn treated with a biologically active substance is 27% higher compared to both controls (untreated and treated with a Placebo bath), its green weight is 25% higher, and the harvest of cobs is 20% higher.
    C. | Experiments in free ground on small businesses.
    In 10x10 cases, maize was planted and a pre-emergence treatment of 50 EC-preparations containing the proposed compound in the form of the racemate according to Example 8 was carried out using 0.1, 1.0, 3.0 or 5.0 kg / ha of this compound. Post-treatment treated with a dose of 1.0 kg / ha. The spray liquid was prepared by diluting the preparation with rain water, using 500 liters of spray liquid per 1 ha. Concentration of the biologically active substance in the spraying fluid, depending on the dose of O5.02-1%, Delki dredged weeds.
    The results are shown in table 4.
    Spreadsheets
    From table 4 it can be seen that the racemate is a biologically active substance with isob
    stint when used for pre-treatment is already effective at a dose of 0 kg / ha, however, the most favorable effect is achieved at doses of 1-3 kg / ha. In this case, the plant is 21-27% higher, green mass is 27 -35% more, corn cob yield is 16-18% more than that of untreated plants, When applied for post-harvest processing of 1.0 kg / ha, the results are much worse,
    PRI me R 9, Test flies (Musca domestica),
    } Adult Musca domestica.
    From a 50% emulsion concentrate, a 3% spray liquid was obtained. From it, they were taken into a glass beaker so much that the bottom of the glass was covered with a layer of 2.5 mg / cm of the racemate of the biologically active substance. 20 specimens of anesthetized CO houseflies (Musca domestica) were placed in the glass. Dichlorfon (0,0-dimethyl-2,2,2-dichlorovinyl-phosphate) in the same doses was used as a comparative substance.
    The results are shown in Table 5.
    Table 5
    five
    0
    five
    J Larvae Musca domestica, For the cultivation of the larvae of houseflies (Musca domestica), a suitable nutrient medium was prepared from the following components: kg wheat bran, 1 l milk, 10 kg fodder yeast and 6 g. Nipadin (P-hydroxybenzoic acid ethyl ester). 200 g of this nutrient medium were added to glass beakers, treated with such an amount of the racemate the biologically active substance so that the concentration in the nutrient medium is 250, 500 or 100 ppm. In this case, the biologically active substance in the form of a 50% emulsion concentrate is added to medium and then homogenized in the latter. We also conducted a control experiment without a biologically active substance. In prepared cups placed 50 larvae of flies at the age of 1 day, the cups were covered with a net from flies. In the assessment, it was determined how many individuals hatched from pupae,% of the control (see Table 6),
     Table 6
    processing 250
    500 1000
    100 29.6
    ABOUT
    About 70.4
    100.0 100.0
    912
    It is obvious from Table 6 that although the effect of dichlorfon is more radical than the effect of the proposed biologically active substance is slower, the toxicity of the latter is significantly lower and it does not have a choline-steroid inhibitory effect.
    Example 10, Growth Stimulating Study,
    ) Experiments in the greenhouse.
    Seeds of the experimental plants were sown in plastic vessels measuring 14x12x x5 cm in washed sand. Compound 2- (propargyloxyimino) .-, 7, 7-trimethylbicyclo (2,2,1) -heptane, dissolved in acetone, was used for a preliminary experiment; B each vessel was sprayed with a solution prepared with 5 ml of acetone Whether so that the amount of active substance corresponds to a dose of 0.1 kg / ha or 0.2 kg / ha. Repeated four times the experience was evaluated on the 32nd day,
    Table 7 shows the height of the plants, correlated with the control plants (100%).



    Table 7
    Plant Plant height at dose, kg / ha
    125.5 124.4
    A6.0 125.0

    62120116298
    5792126275
    479890235
    10 Prodolzhe1P {e tabl. 7
    Plant
    Plant height at the dose, kg / ha
    0.1,
    behind
    nothing


    chuck
      R i J 4 130, 5
    116.4 1 17.2 122.0
    120.5 107.3
    , 25.0 127.0
    105.5 159.4 119.5
    130.8 147.0
    15 20
    five
    thirty
    five
    0
    } Experiments in open ground on small plots of land (80 m,
    The compound of a) was used for pre-emergence treatment at doses of 0.2, 0.5 or 1.0 kg / ha (300 l of water per hectare and sprayed onto tomato culture in sandy and clayey soil. During the growing season Three harvesting of ripe fruit was carried out. Throughout the experiment, the land was free from weeds.
    Results are c.
    For comparison, a known leaf fertilizer of the following composition was used - trace elements,%: N 12; four; KjO 6; Mg trace elements; Mp; Fe; Si; Mo; AT; Co; Zn.
    T a b
    faces
    eleven
    с1 Experiments in open ground using logyphmically increasing dose. ,,
    On plots of size 20 x x 2 m, various plant species were treated both in the pre-emergence and post-emergence conditions with substances with doses of 0.15–8.9 kg / ha under paragraph a) aKTHBHdro of the substance. Processing in the post-emergence state was performed in this case, when; 1 plants had a height of 15–20 cm. All land areas are medium yellow loam.
    C) Plant height (corn, sunflower) compared to untreated control plants.
    In the pre-emergence treatment, the height was measured on the. Day after sowing, in the post-emergence treatment, on the 20th day after treatment,
    Each value is an average of 5 measurements on a plot of 20 x x2pog.m. (s: m.tabl, 9). .
    .Table 9
    Corn
    -2- (propargyloxyimino) -1, 7,7-triCj) The total weight of corn plants is 55 methylbicyclo (2.2.1) heptane. - and the weight of corn cobs,% to control plants is given c) The weight of the fruits of the beans,% to the control, 10, but, is given in table 12.
    12
    Lu table
    8.9 142.3 -128.4 112.1 115 4.5 151, 1 .125.7 105.3 1 19.2 2.8 122.5 115.0 122.3 105-, 3
    Cj) Fruit weight of tomatoes,% of the control is given in Table II,
    25
    Table 11
    35
    1 1248532
    Table 12
    152,1115,7105,1132,5
    151,5121,097,8129,7
    158,4126,3110,1114,8
    142,1110,5102,5149 „9
    121,0121,098,9140,0
    147,3121,0105,3I25J
     2- (propargyloxyimino) -157,7-trimethylbicyclo (2.2.1) -heptane,
    Cj) The weight of cucumber fruits,% of the control (processing only in the pre-emergence state) is given (see tab. 13),
    Table 13
    Order 4144/60 Circulation 379 Subscription VNIIPI USSR State Committee
    for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab. 4/5
    -Production and printing company, Uzhgorod, ul, Project, 4
    14
    Continuation of table 13
    4.5 3.6 2.8
    109.2 16.2
    1 18.7
    108.1 102.7 I 14.2
    Example 1 I (comparative), Compound 2-cyanobic acid (2,2,1) -heptane, the effect of which is tested on legumes. The test was carried out according to example 8; Results are given in Table 14.
    Table 14
    2-Cyanobicyclo (2,2,1) -heptane - known soy
    权利要求:
    Claims (4)
    [1]
    one . The method of obtaining 2- (propargyloxyimino) -1, 7,7-trimethylbicyclo · (2,2,1) -heptane of the formula (P in the form of a racemate or optically active antipode, characterized in that the racemate or optically active derivative 1,7 , 7-trimethylbicyclo (2,2,1) -heptane of the formula (II) where Y is oxygen, sulfur or an oxime group, is reacted with a propine derivative of the formula
    R-CH 2 -C = CH 2 , (III) where R is a halogen or aminooxy group, provided that if Y is oxygen or sulfur, R is an aminooxy group, and if Y is an oxime group, R is a halogen, or acid addition salt in the presence of a condensing agent and an organic solvent, followed by isolation of the target product in the form of a racemate or optically active antipode.
    [2]
    2, The method according to claim 1, characterized in that the pyridine of formula II, where Y is oxygen or sulfur, is used as a condensing agent.
    [3]
    3, Pop method, 1, characterized in that alkali, sodium methylate, sodium amide or sodium hydride are used as a condensing agent according to formula II, where Y is an oxime group,
    [4]
    4, Method 1, characterized in that lower alcohols, aromatic hydrocarbons, dimethylformamide or a mixture of xylene and dimethylformamide are used as an organic solvent.
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    同族专利:
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    HUEE002589|HU181873B|1978-08-22|1978-08-22|Plant growth regulating and/or insecticide composition containing 2-/propagyl-oxy-imino/-1,7,7-trimethyl-byciclo/2.2.1/heptane further process for preparing the active suastance|
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