• 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:
    Vitamin A alcohol and its lower alkanoic esters are prepared by desulphonation of corresponding sulphones with a solid potassium alcoholate of a primary or secondary lower alcohol at 10 DEG to 50 DEG C. in an anhydrous liquid hydrocarbon.
    公开号:SU722483A3
    申请号:SU772504519
    申请日:1977-07-26
    公开日:1980-03-15
    发明作者:Декор Жан-Пьер
    申请人:Рон-Пуленк Эндюстри (Фирма)；
    IPC主号:
    专利说明:

    one
    This invention relates to an improved process for the preparation of vitamin A derivatives of total formula 1.
    .xHH..x With “goK.
    where R is a hydrogen atom or a radical
    COR, wherein R is alkyl Cj-Cfe. A known method for producing vitamin A derivatives of the general formula T by desulfonating the sulfone of the general formula P
    SOjAP
    SNGOV
    where COCHj, Ar- phenyl,
    alcohol alkali metals in an alcohol medium at 80 ° C for 4-16 h 1). Such processing conditions are little compatible with the poor stability of the target product. The disadvantage of this method is also the somewhat longer process time.
    The closest to the proposed method is to obtain vitamin A derivatives of general formula D by desulfonating the sulfone of general formula il
    Ojar
    CHjOB
    ten
    where R is a hydrogen atom or the radical COR, in which R is alkyl Ci-O, Ar is phenyl,
    potassium tert-butylate in tetrahydrofuran or pyridine at 20 s 2. The process takes 16-20 hours.
    The disadvantage of this method is the long duration of the process.
    The aim of the invention is to reduce the duration of the process.
    The goal is achieved by the proposed method of obtaining derivatives A of general formula D by desulphonating a sulfone of general formula II,
    where R and Ar have the indicated meanings, alkali metal alkoxides, followed by isolation of the target product as an alcohol or ester. A distinctive feature of the proposed method is to conduct the process at 10–50 ° C using methylate or ethylate or potassium isopropylate as an alcoholate, an alkali metal or as a suspension in anhydrous cyclohexane or hexane at the molar ratio of the starting sulfone and alkali alcoholate metal equal to 1: 3-5. Under these conditions, the product yield is about 90%. When a sulfon of general formula II in which R is a hydrogen atom is desulfonated, since the resulting product of the corresponding general formula I is relatively unstable, it is preferred to be directly converted into a product of general formula 1 in which R is the COR radical mentioned above, with using esterification by any known method, for example, in a liter round-bottom flask, which is in a dark place, load 350 cm of ethanol and 7.05 g (15-10 mol) of the sulfonacetate of formula II in an argon atmosphere and mix the resulting mixture. The dissolution of sulfoch is incomplete. After 10 minutes of stirring, add 140 cm of an aqueous solution with 1% potash (25-10 mol) and continue mixing at a temperature of about 25 ° C, which leads to the complete dissolution of the sulfonate. After 45 minutes of stirring, it was checked by chromatography in thin c (eluant: hexane-tert-butanol, 9: 1 according to 5 records) that the sulfonate was completely saponified into sulfon alcohol. Then ethanol is distilled under reduced pressure at 45 ° C; the residual turbid aqueous solution is recovered, 350 cm of anesthetic ether is introduced into it, washed with 50, then dried on sodium sulfate, using the end of the walkie-talkie under reduced pressure at a temperature of approximately 25 s for 2 h 15 min, ending at 0, 1 mm Hg, the residue is obtained - 6.7 g of a pale yellow oil, consisting of the sulfonic alcohol of formula P. This sulfonic alcohol is dissolved in 200 cm of anhydrous diclohexane at 28 ° C. The resulting solution was kept under argon and 3.655 g of dry potassium methylate (52) was added and the suspension was stirred. The liquid phase is painted in light lilac color, while the temperature rises to. After 1 h stirring with thin layer chromatography, it was checked that the sulfon alcohol disappeared. The light brown reaction mixture is cooled to, then 140 cm of salt water is added dropwise. The organic phase is separated from the liquid phase and extracted twice with a total amount of 200 cm of hexane. The various organic phases are combined, washed with a total amount of 120 cm-water (4 times), then 30 cm of salt water, then a few drops of pyridine- are added to them, dried on sodium sulfate and concentrated under reduced pressure at approximately 25 ° C to until the residual volume is 150 cm. To the resulting solution is added under argon and in a dark place 1.985 g of pyridine and 3.006 g of acetic anhydride, add up to 200 CM with the addition of anhydrous hexane and heat the mixture at 4 hours 30 min. It is then checked by thin layer chromatography that all the alcohol has been converted to acetate. The reaction mixture is cooled to 5 ° C, 70 cm of hexane is added to it, then 110 cm of water are added over 10 minutes, maintaining the temperature at 5 ° C. The organic phase is separated, washed successively with 35 cm of water containing 7 drops of concentrated sulfuric acid with water containing 14 drops of soda 10 n, finally 2 times with neutral using 30 cm of salt water until neutral. After adding 0.21 g of ditert-butylhydroxytoluene, used as a stabilizer, drying on sodium sulfate and concentration under reduced pressure at 35–40 ° C, ending at a pressure of 0 mm, 1 mm Hg. 5.299 g of untreated vitamin A is obtained, the percentage of which (determined by nuclear magnetic resonance, ultraviolet spectrography and liquid chromatography at high speed) is 86%, which corresponds to a 87% yield of vitamin A units relative to the starting sulfonacetate. Example 2. To 20 cm of anhydrous hexane maintained at 28 ° C, 0.94 g {210 mol) of sulfonacetate of formula II are added under argon and the mixture is vigorously stirred to distribute the sulfonate well. Then 0.7 g of potassium isopropylate (7) is added in one portion through a funnel and the funnel is washed with 5 cm of anhydrous hexane. The temperature of the mixture rises to 30-31 ° C and then again drops to 28 ° C. After 40 minutes of stirring with thin layer chromatography, it is checked that the desulfonation is complete. Then until
    权利要求:
    Claims (1)
    [1]
    Claim
    A method of obtaining derivatives of Vitamin.min And the General formula
    Ch g 0H where R - a hydrogen atom or a radical COR *, wherein R * - Ctputem desulfonaTsii alkyl sulfone of formula Ar 0 r
    HE
    Ca where R - has the indicated values, Ar - phenyl, alkali metal alkoxides, followed by isolation of the target product in the form of alcohol or ether, characterized in that, in order to reduce the duration of the process, the latter is carried out at 10-50 ° C using as alkali metal alkoxides of methylate or ethylate or potassium isopropylate in solid form or as a suspension in anhydrous cyclohexane or hexane, with a molar ratio of the starting sulfone and alkali metal alcoholate of 1: 3-5.
    类似技术:
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    同族专利:
    公开号 | 公开日
    DE2734172A1|1978-02-02|
    HU173649B|1979-07-28|
    CA1080242A|1980-06-24|
    BE857236A|1978-01-27|
    JPS5315341A|1978-02-13|
    NL187353C|1991-09-02|
    US4175205A|1979-11-20|
    CH623305A5|1981-05-29|
    JPS5953903B2|1984-12-27|
    IT1085596B|1985-05-28|
    FR2359821A1|1978-02-24|
    NL187353B|1991-04-02|
    NL7708083A|1978-01-31|
    GB1532915A|1978-11-22|
    FR2359821B1|1978-12-15|
    DE2734172C2|1987-11-05|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    FR2138212B1|1971-05-19|1973-05-11|Rhone Poulenc Sa|
    BE794872A|1972-02-02|1973-08-01|Rhone Poulenc Sa|NEW SULPHONES DERIVED FROM DIMETHYL-1,5 HEXADIENE-1,5 YLENE|
    BE794944A|1972-02-04|1973-08-02|Rhone Poulenc Sa|NEW UNSATURATED SULPHONES CONTAINING A CARBONYL FUNCTION|
    FR2205898A5|1972-11-08|1974-05-31|Rhone Poulenc Sa|
    US3960967A|1973-09-14|1976-06-01|Hoffmann-La Roche Inc.|Process for producing a sulfone derivative of vitamin A alcohol|BE794872A|1972-02-02|1973-08-01|Rhone Poulenc Sa|NEW SULPHONES DERIVED FROM DIMETHYL-1,5 HEXADIENE-1,5 YLENE|
    JPS54182007U|1978-06-13|1979-12-24|
    US4523042A|1983-07-29|1985-06-11|Usv Pharmaceutical|Derivatives of alpha-alkyl polyolefinic carboxylic acid useful in the treatment of psoriasis|
    FR2573074B1|1984-11-13|1987-01-30|Rhone Poulenc Sante|PROCESS FOR PREPARING RETINONITRILE|
    EP0187259B2|1985-01-10|1996-05-15|Kuraray Co., Ltd.|Process for producing vitamin A or its carboxylic acid esters, and intermediate compounds useful for the process|
    TW252974B|1993-03-23|1995-08-01|Takeda Dharm Industry Co Ltd|
    DE19926090A1|1998-06-12|1999-12-16|Sumitomo Chemical Co|Production of retinal, useful as carotinoid intermediate, via new sulfonated aldehyde intermediates|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR7622992A|FR2359821B1|1976-07-28|1976-07-28|
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