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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1650066생성일: 2026년 10월 27일

Hydrochloric Acid → 5-Methyl-4-(2-propenyl)-2-phenylsulfenylcyclohexanone

https://huagongshe.com/reaction/1650066

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium hydrideHCID 82127—
반응물Methyl benzenesulfinateHCID 2759784—
반응물(3R,4S)-3-Methyl-4-(prop-2-en-1-yl)cyclohexan-1-oneHCID 15670663—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-Methyl-4-(2-propenyl)-2-phenylsulfenylcyclohexanoneHCID 19855336—

반응 조건

온도0 °C

반응 단계

To a 0° C. mixture of 16.9 g. (0.109 mole) of methyl benzenesulfinate and 8.68 g. (0.217 mole) of potassium hydride in 100 ml. of dimethoxyethane was slowly added a solution of 15.0 g. (0.0987 mole) of trans-3-methyl-4-(2-propenyl)cyclohexanone in 50 ml. of dimethoxyethane. The reaction was stirred 30 minutes longer at 0° C. and then cautiously added to 500 ml. of ice-saturated sodium chloride and 45 ml. 6N hydrochloric acid. The quenched reaction mixture was extracted once with 300 ml. ether and once with 200 ml. dichloromethane. The organic extract was dried over magnesium sulfate and evaporated to give a quantitative yield of the title compound as a semisolid mixture of axial and equatorial sulfenates. Crystallization from ether yields 7.8 g. of pure axial sulfenate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04921994
출처 데이터셋uspto-grants-1990_05
ORD IDord-e3ba299f00b44733bd756c1fc9a27b05
출처 메모uspto-grants-1990_05