Process for producing isothiuronium salts of phosphorous acid
专利摘要:
A composition for combatting fungal and bacterial diseases in plants is disclosed which contains, as the active ingredient, a compound of the formula: <IMAGE> in which: R1 is hydrogen or an alkyl radical containing from 1 to 6 carbon atoms, R2 is an alkyl radical containing from 1 to 18 carbon atoms, R1 and R2 can additionally form an ethylene or propylene chain which is optionally substituted by alkyls containing from 1 to 3 carbon atoms, and R3 and R4, which are identical or different, are hydrogen, an alkyl radical containing from 1 to 18 carbon atoms, a cycloalkyl radical containing from 3 to 7 carbon atoms, an alkenyl radical containing from 3 to 18 carbon atoms, the phenyl radical or the benzyl radical, in association with an inert carrier which is acceptable in agriculture. 公开号:SU952107A3 申请号:SU802891756 申请日:1980-03-11 公开日:1982-08-15 发明作者:Абблар Жак;Мишель Голлиар Жан;Лакруа Ги 申请人:Рон-Пуленк Агрошими (Фирма); IPC主号:
专利说明:
R has the indicated meanings or R and R together form a chain of ethylene or propylene, with an isothiuroni halide of the general formula. 5K, CRH where R has the indicated meanings; X is halogen, at 80-100 ° C ... The described method allows obtaining isothiuronic salts of phosphorous acid of formula I in high yield. The method is suitable for lower alkyl phosphites, but it is difficult to practically implement it to obtain the isothiuronium salts of higher alkyl phosphites. The compounds obtained are purified by recrystallization from acetone, hexane, cyclohexane or petroleum ether in the case when they are solids, or distillation in a vacuum — when they are oily liquids. Example 1. Preparation of methylphosphite 5-ethyl-M dodecylisothiuroni. A mixture of 19 g (0.035 mol) of S-ethyl-N-dodecylisothiuronium iodide and 4.4 g (0.04 mol) of dimethyl phosphite is gradually heated. When methyl iodide begins to be distilled. The temperature of the reaction mixture is maintained at 90-95 ° C for 15 minutes, then it is raised to 50 ° C. Next, the reaction mass is dissolved in 100 ml of acetone, cooled in a bath with a mixture of acetone and ice. As a result of cooling, the target product precipitates. The precipitate is filtered off, washed with 20 ml of cold acetone, squeezed and dried in vacuum at room temperature. temperature A white solid is obtained with a yield of 82% (relative to 8-ethyl-L-dodecylisothiuronium iodide). Other compounds of the formula I are prepared in a similar manner. The physicochemical characterization of all the products obtained is presented in the table. and about Yu g 1P rf az and but: sh 0 fO tc az CJ and go y o: o aw and az and (ABOUT About ace o about SP go cm well I ft f} about rf SU c S h X az az with J about about ct and tsg and go YY) P az and az and az and and LO Li az SU t ABOUT and and and :( 1L ) VO go go p 00 (P VO N CO about h yv CO cm och tN n t r cs n n about four oo n 00 n in rH "L about about g n R oh oh a: tn ; and 33 with and m EU and about 00 th g yu go 1/1 w 1 00 1L about coke t with hhh about R | oo r-t with (L about g g n VO 1L 1L D) N go g- { about f about 00 about MS vH Ti oo 1L N U1 cm “Ao n D) 1L about 00 00 00 with 40 V CM 00 about o see about PM g VO 00 MS 1L 00 H ate PM ON (L about MS with CM 1L 00 about H n chin H about VO H tg "-I g sh in P VO H 1L. 1I 1L 00 VO goo but oo ° s Zy §0 one 00 5H one SP (L g g her her "oh gcd about and and (R x X LO X SP gi about and "" go t x x X about and and with sgk and X o about R SP J "The formula of the invention 1. The method of obtaining the isothiourony of phosphorous acid salts of the general formula I L B. Ь- :) igR BiO-p-0 K (, H where R is hydrogen or alkyl Rn is alkyl. ; Rj is hydrogen, alkyl, CI logex, phenyl, benzyl, isopropenyl, or CH- (CH) g; R. is hydrogen, alkyl, cyclic hexyl, or benzyl, and R and R4 cannot simultaneously denote hydrogen with R - alkyl and Ri2 - a kil C, -C, 3 are included in the dialkyl phosphite of the general formula xCho where R is methyl or ethyl; R - has the indicated values or R and R together form an ethylene chain or Pilen, subjected to interaction with the halide isothiuroni General formula VLT.V) 51, CC. where RQi, R3, R4 have the indicated meanings; X - halogen, with SO-lOO C. Sources of information taken into account during the examination 1.Orlovsky V.V., Vovsi B, A. On the question of the interaction of dialkylphosphites with thiourea. ZHOKH, 1969, 39, 6., 1259. 2.Orlovsky, V.V., Vovsi, B.A., Mishkevich, A.E. On the dealkylation of dialkyl esters of phosphorous acid, Oh, 1972, 42, 1930.
权利要求:
Claims (1) [1] Claim 1. A method of producing isothiuronium salts of phosphorous acid of the general formula I where HZ is hydrogen or alkyl C ^ -Cz; R ^ is alkyl C ^ -C, ( ^, moreover, they can form a chain of ethylene or propylene; R 3 is hydrogen, alkyl C 3 -C iS , cyclohexyl, phenyl, benzyl, isopropenyl or C 0 NCHS = CH- (CH g ) c ; R ^ - is hydrogen, alkyl and C -C _ 12 cyclohexyl or benzyl, wherein R 20 3 and R 4 may not simultaneously denote hydrogen when R ^ - Cj-Cj alkyl, and C - alkyl-SO 4, s-CLA in yuchayuschiysya the fact that 25 dialkylphosphite of the general formula l w / h 0 where R is methyl or ethyl; R-, - has the indicated meanings, or R and R 4 together form an ethylene or propylene chain, are reacted with a halide of the formula isothiuronium with a total R <i , R 3 ' R 4 have the indicated meanings; X is halogen 80-100 ° C.
类似技术:
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同族专利:
公开号 | 公开日 CH640700A5|1984-01-31| AR220747A1|1980-11-28| DE2910237C2|1987-04-09| PH16323A|1983-09-05| IL56884A|1983-11-30| ATA197179A|1983-09-15| ZA791224B|1980-03-26| TR19935A|1980-05-02| IT1162483B|1987-04-01| ES478641A1|1979-11-01| RO79037A|1983-07-07| LU81055A1|1980-09-24| JPS6247842B2|1987-10-09| CA1118785A|1982-02-23| JPS54130521A|1979-10-09| CS208492B2|1981-09-15| IT7948373D0|1979-03-15| DK106679A|1979-09-17| GB2016926B|1982-07-28| PL214137A1|1979-12-03| AU4516279A|1979-09-20| AU530215B2|1983-07-07| DE2910237A1|1979-10-04| GR68033B|1981-10-27| NZ189907A|1982-03-09| BG32264A3|1982-06-15| EG14428A|1983-12-31| SE446929B|1986-10-20| SE7902354L|1979-09-17| CU35057A|1982-08-24| IE48734B1|1985-05-01| FR2419675A1|1979-10-12| BR7901620A|1979-10-16| GB2016926A|1979-10-03| HU182985B|1984-03-28| NL7902056A|1979-09-18| IE790614L|1979-09-16| AT374483B|1984-04-25| NL188831C|1992-10-16| BE874907A|1979-09-17| JPS62281886A|1987-12-07| PT69356A|1979-04-01| OA06216A|1981-06-30| DD142282A5|1980-06-18| US4382928A|1983-05-10| ES480224A1|1980-02-01| IL56884D0|1979-05-31| RO79037B|1983-06-30| FR2419675B1|1980-11-14|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US4119724A|1973-11-26|1978-10-10|Pepro|Fungicidal compositions containing phosphorous acid and derivatives thereof| FR2254276B1|1973-12-14|1977-03-04|Philagro Sa| FR2380286B1|1977-02-14|1980-01-11|Philagro Sa|FR2457873B1|1978-03-16|1984-06-22|Rhone Poulenc Agrochimie| FR2451164B2|1978-03-16|1981-05-22|Rhone Poulenc Agrochimie| FR2655816B1|1989-12-14|1994-04-29|Rhone Poulenc Agrochimie|DISPERSABLE GRANULES OF FUNGICIDE PRODUCTS.| US5133891A|1990-04-27|1992-07-28|Rhone Poulenc Ag Co.|Treatment of plants for frost protection| JPH0478737U|1990-11-19|1992-07-09| US6160008A|1996-09-26|2000-12-12|Meditor Pharmaceuticals Ltd.|Pharmaceutical compositions comprising S-alkylisothiouronium derivatives| HU0302362A3|2000-09-05|2005-05-30|Meditor Pharmaceuticals Ltd|Pharmaceutical compositions for headache, migraine, nausea and emesis|
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申请号 | 申请日 | 专利标题 FR7808237A|FR2419675B1|1978-03-16|1978-03-16| 相关专利
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