SU652888A3 - Method of obtaining sulfonoalcohol esters - Google Patents

Method of obtaining sulfonoalcohol esters

Info

Publication number
SU652888A3
SU652888A3 SU752112822A SU2112822A SU652888A3 SU 652888 A3 SU652888 A3 SU 652888A3 SU 752112822 A SU752112822 A SU 752112822A SU 2112822 A SU2112822 A SU 2112822A SU 652888 A3 SU652888 A3 SU 652888A3
Authority
SU
USSR - Soviet Union
Prior art keywords
obtaining
esters
sulfonoalcohol
formula
chgor
Prior art date
Application number
SU752112822A
Other languages
Russian (ru)
Inventor
Мене Альберт
Жюлиа Марк
Original Assignee
Рон-Пуленк С.А. (Фирма)
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Рон-Пуленк С.А. (Фирма) filed Critical Рон-Пуленк С.А. (Фирма)
Application granted granted Critical
Publication of SU652888A3 publication Critical patent/SU652888A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/44Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

.., , I..,, I

Изобретение огноситса к способу по лучени  новых химических соединений сложных эфиров сульфоноспйртов общей формулыThe invention of fireproofing to the method of obtaining new chemical compounds of esters of sulfonic spirits of the general formula

RSOgCHg - СХ « СУ - CHgOR (1)RSOgCHg - CX "SU - CHgOR (1)

где дюбой из X И У означают один - мегилыЕый радик.ад, другой - атом водороца;where the dyube of X and Y means one — a megiley radic. ad, the other — an atom of hydrogen;

. I - алкил, аралкйл, алкиларил, замещенный или незамещенный арил;. I is alkyl, aralkyl, alkylaryl, substituted or unsubstituted aryl;

R -.ац;ип - CORg , где R,; - атом . водорода или алкил, или арил.R -.ац; un - CORg, where R ,; - atom. hydrogen or alkyl, or aryl.

Эфнры сульфоноспйртов предсгавл юг интерес в качестве вьгсокореакпионноспособных полупродуктов оргадаческого синтеза С Их .помощью можно получать пищевые .красители и фармацевтические про дукты.Efnry of sulphonic spirits predgavl yug interest as vyogorekorespionnohnyh intermediates of organic synthesis With Their. Help can be obtained food. Dyes and pharmaceutical products.

Известен способ получени  соединенийA known method for producing compounds.

обшей формулы general formulas

XCeHgOCHOHSOaQHs ,XCeHgOCHOHSOaQHs,

где X - атом водорода, метал, путем взаимодействи  феннлсульфохлорида с винил арнловым эфиром с последунЬшнм окис Ленйем образующегос  продукта перуксуоной КИСЛОТОЙ при охлаждении. Полученные эфйры сульфонов 1могут быть испопьзова-. ны в качестве полупродуктов органического синтеза 1 | . Однако в литературе нет сведений 6 .способе получени  соединеннй формулы (1) Новые соединени  - . эфйры сульфоноспйртов обшей формулы (IJwhere X is a hydrogen atom, metal, by reacting fennsulfochloride with vinyl arnyl ether with the subsequent oxide Leneum of the product formed by the peroxoic ACID upon cooling. The resulting ethers of sulfones 1 can be used. as intermediates for organic synthesis 1 | . However, in the literature there is no information. 6. A method for obtaining the compound of the formula (1). ethers of sulfonic spirits of the general formula (IJ

в отличие от известных аналогов coijep-. жат реакционноспособную метиленовую группу, несущую сульфоновую функцию, в св зи с чем оии могут реагировать, например , ,с алкилгалогейидами или сопр жевными диолефи нами. Так с алкилгалогвнидом , например хлоридом, соответсгвуюншм формулйЦСК, где  вл етс  углеводородным радикалом, реакци  приводит к соединению формулы Q - CHg. () СУ - CHgOR , которое затем путем десульфировани  с помощью щелочного агента может превращатьс  в соединение , соответствующее формулеin contrast to the known coijep- analogues. A reactive methylene group bearing a sulfonic function, in connection with which oii can react, for example, with alkylhaloids or conjugated diolefins. So with an alkyl halide, e.g. chloride, corresponding to the formula CSC, where it is a hydrocarbon radical, the reaction results in a compound of the formula Q - CHg. () SU-CHgOR, which then can be converted by desulfurization with an alkaline agent to a compound corresponding to the formula

Q СНа ( S CfeR) - СХ « Cy-CHgOR,Q СНа (S CfeR) - СХ «Cy-CHgOR,

SU752112822A 1972-12-07 1975-03-17 Method of obtaining sulfonoalcohol esters SU652888A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7243582A FR2210187A5 (en) 1972-12-07 1972-12-07 1-Sulphomyl-but-2-ene-4-ols and their esters - as intermediates for drugs perfumes and food colours

Publications (1)

Publication Number Publication Date
SU652888A3 true SU652888A3 (en) 1979-03-15

Family

ID=9108349

Family Applications (1)

Application Number Title Priority Date Filing Date
SU752112822A SU652888A3 (en) 1972-12-07 1975-03-17 Method of obtaining sulfonoalcohol esters

Country Status (3)

Country Link
BE (1) BE808326A (en)
FR (1) FR2210187A5 (en)
SU (1) SU652888A3 (en)

Also Published As

Publication number Publication date
FR2210187A5 (en) 1974-07-05
BE808326A (en) 1974-06-06

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