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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 616814생성일: 2026년 10월 27일

Sulfur Dioxide → 3-Chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester

https://huagongshe.com/reaction/616814

반응식

참여 물질

역할이름HCID투입량
반응물Sulfur DioxideHCID 1119—
반응물Sulfuryl chlorideHCID 24648—
반응물Diethyl ((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl)phosphonateHCID 70421—
촉매PyridineHCID 1049—
용매Carbon TetrachlorideHCID 5943—
생성물3-Chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl esterHCID 86735499—

반응 조건

온도0 °C

반응 단계

71.2 g of 3,5-di-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester are dissolved in 200 ml of carbon tetrachloride. After addition of a few drops of pyridine, 40.5 g of sulphuryl chloride are added dropwise, with stirring, at about 0° C in the course of 45 minutes. The reaction mixture is then further stirred for 10 hours at room temperature, in the course of which the formation of sulphur dioxide is observed. After the reaction is terminated, the solvent is removed as far as possible completely in vacuo. The semi-crystalline residue is digested with water and washed neutral and finally recrystallised from aqueous isopropanol in order to purify it. Instead of isopropanol it is also possible to use ethylene glycol monomethyl ether. Toluene is also suitable for effecting recrystallisation, but the crude product must in this case be freed from water beforehand. The 3-chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester is obtained in the form of colourless crystals (stabiliser 1) with a melting point of 116° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04076690
출처 데이터셋uspto-grants-1978_02
ORD IDord-990654cce92842b785073a598741315f
출처 메모uspto-grants-1978_02