戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1284442作成日:2026年10月27日

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

https://huagongshe.com/reaction/1284442

反応式

関与物質

役割名称HCID仕込み量
反応物CrotonaldehydeHCID 447466—
反応物5-Methyl-2-hepten-4-one (natural)HCID 517791—
反応物HCID 178456030HCID 178456030—
溶媒Diethyl EtherHCID 3283—
生成物5-Methyl-2-hepten-4-olHCID 54181019—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04563365
出典データセットuspto-grants-1986_01
ORD IDord-b05f49280dfa45a08efce111e69dd9ac
出典メモuspto-grants-1986_01