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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906701Generated: October 25, 2026

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

https://huagongshe.com/reaction/1906701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCrotonaldehydeHCID 447466—
Reactant5-Methyl-2-hepten-4-one (natural)HCID 517791—
ReactantHCID 178456030HCID 178456030—
SolventDiethyl EtherHCID 3283—
Product5-Methyl-2-hepten-4-olHCID 54181019—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654168
Source datasetuspto-grants-1987_03
ORD IDord-59d12fc1e4514907a882ff8d9ed6f989
Source noteuspto-grants-1987_03