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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256620생성일: 2026년 10월 26일

Acetaldehyde → Methyl 2-cyclohexyl-3-hydroxypropanoate

https://huagongshe.com/reaction/256620

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물DiisopropylamineHCID 7912—
반응물Cyclohexaneacetic acid, methyl esterHCID 139743—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Methyl 2-cyclohexyl-3-hydroxypropanoateHCID 19785625—

반응 단계

To a stirred solution of diisopropylamine (0.85 ml, 6.10 mmol) in 30 ml tetrahydrofuran at -78° under argon was added n-butyllithium (2.5 ml of a 2.5M solution in hexane). After 0.5 hour, methyl cyclohexylacetate (1 ml, 6.10 mmol) was added dropwise in 10 ml tetrahydrofuran. The solution was stirred for 45 minutes, after which was added acetaldehyde (1 ml) in 10 ml tetrahydrofuran. This solution was stirred for two hours at -78°, warmed to room temperature and stirred an additional 12 hours, quenched with water and acidified with 10% hydrochloric acid. The mixture was extracted twice with ethyl ether, and the combined organic portions were then washed once with 10% hydrochloric acid, twice with water, once with saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give the alcohol as an orange oil (b.p. 85°-92°, 0.5 mm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258400
출처 데이터셋uspto-grants-1993_11
ORD IDord-8c435af331554cb1a715c2d7473bf652
출처 메모uspto-grants-1993_11