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HRID 1906701作成日:2026年10月26日

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

https://huagongshe.com/reaction/1906701

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-butylmagnesium bromide (prepared, for example, from 2-bromobutane 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US04654168
出典データセットuspto-grants-1987_03
ORD IDord-59d12fc1e4514907a882ff8d9ed6f989
出典メモuspto-grants-1987_03