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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1284442Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1284442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCrotonaldehydeHCID 447466—
Edukt5-Methyl-2-hepten-4-one (natural)HCID 517791—
EduktHCID 178456030HCID 178456030—
LösungsmittelDiethyl EtherHCID 3283—
Produkt5-Methyl-2-hepten-4-olHCID 54181019—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04563365
Quelldatensatzuspto-grants-1986_01
ORD IDord-b05f49280dfa45a08efce111e69dd9ac
Quellennotizuspto-grants-1986_01