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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444113생성일: 2026년 10월 24일

Allyl chloride → alpha-Allyl-4-methyl-3-cyclohexene methanol

https://huagongshe.com/ko/reaction/444113

반응식

참여 물질

역할이름HCID투입량
반응물Allyl chlorideHCID 7850—
반응물TetrahydrofuranHCID 8028—
반응물3-Cyclohexene-1-carboxaldehyde, 4-methyl-HCID 111012—
반응물MagnesiumHCID 5462224—
용매TolueneHCID 1140—
생성물alpha-Allyl-4-methyl-3-cyclohexene methanolHCID 2056153565.2%

반응 조건

온도71 °C

반응 단계

A solution of 251 grams (3.3 moles) of allyl chloride and 372 grams (3 moles) of 4-methyl-3-cyclohexenecarboxaldehyde is added dropwise to a stirred slurry of 77 grams of magnesium (3.2 moles) and 1500 ml of tetrahydrofuran at reflux under nitrogen over a three-hour period. The reaction mixture is heated at reflux (71° C.) for 30 minutes after the feed is complete, whereupon 500 ml of toluene is added. A distillation head is attached to the reaction flask and the tetrahydrofuran is distilled off at atmospheric pressure to a pot temperature of 100° C. The remaining organic solution is cooled to 0° C., whereupon 1000 ml of 18% hydrochloric acid solution is slowly added with external cooling. Two clear layers is formed. The aqueous layer is discarded and the organic layer is quickly distilled. The distillate is fractionally redistilled through a 1.5"×12" Goodloe packed column to afford 325 grams of alpha-allyl-4-methyl-3-cyclohexene methanol (b.p. 92° C., 3.0 mm Hg pressure).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04263149
출처 데이터셋uspto-grants-1981_04
ORD IDord-120aeb7e7f5346edac5e30bb1e7731ac
출처 메모uspto-grants-1981_04