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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1284442생성일: 2026년 10월 26일

Crotonaldehyde → 5-Methyl-2-hepten-4-ol

https://huagongshe.com/reaction/1284442

반응식

참여 물질

역할이름HCID투입량
반응물CrotonaldehydeHCID 447466—
반응물5-Methyl-2-hepten-4-one (natural)HCID 517791—
반응물HCID 178456030HCID 178456030—
용매Diethyl EtherHCID 3283—
생성물5-Methyl-2-hepten-4-olHCID 54181019—

반응 단계

5-Methyl-hept-2-en-4-one to be used according to the invention can be obtained for example by reacting 2-butyl-magnesium bromide (prepared, for example, from 2-bromo-butane and magnesium filings) with crotonaldehyde in ether solution. 5-Methyl-hept-2-en-4-ol is obtained as an intermediate and is oxidized with a mixture of sodium dichromate and sulphuric acid to give 5-methyl-hept-2-en-4-one. The 5-methyl-hept-2-en-4-one is obtained as a mixture of the cis- and trans-isomers, with the latter predominating. The isomer mixture can be separated into the cis-isomer and trans-isomer by simple methods of separation, such as, for example, fractional distillation by a packed column or slotted tube column or preparative gas chromatography. However, it has been found that the use of the individual isomers offers no advantages over the use of the mixture.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04563365
출처 데이터셋uspto-grants-1986_01
ORD IDord-b05f49280dfa45a08efce111e69dd9ac
출처 메모uspto-grants-1986_01