참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium hydride | HCID 82127 | — |
| 반응물 | Methyl benzenesulfinate | HCID 2759784 | — |
| 반응물 | (3R,4S)-3-Methyl-4-(prop-2-en-1-yl)cyclohexan-1-one | HCID 15670663 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | 5-Methyl-4-(2-propenyl)-2-phenylsulfenylcyclohexanone | HCID 19855336 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04921994 |
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| 출처 데이터셋 | uspto-grants-1990_05 |
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| ORD ID | ord-e3ba299f00b44733bd756c1fc9a27b05 |
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| 출처 메모 | uspto-grants-1990_05 |
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