Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 65808Erstellt: 24. Oktober 2026

4-(Acetyloxy)-2-butanone → 2,3,6-Trimethylcyclohex-2-en-1-one

https://huagongshe.com/de/reaction/65808

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Acetyloxy)-2-butanoneHCID 139100—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
Produkt2,3,6-Trimethylcyclohex-2-en-1-oneHCID 3016843—

Reaktionsschritte

130 g of 1-acetoxybutan-3-one and sodium methylate solution in methanol are dripped in the course of one hour from separate supply vessels while stirring into 400 g of boiling diethyl ketone at such a rate that the reaction mixture remains constantly alkaline. A total of 190 g of a 30% by weight sodium methylate solution is used up in this way. The whole is then heated under reflux for another hour and then neutralized with glacial acetic acid. Deposited sodium acetate is filtered off and the filtrate is subjected to fractional distillation. 81 g of 2,3,6-trimethyl-2-cyclohexen-1-one is obtained as well as traces of 4-methyl-3-ethyl-2-cyclohexen-1-one. The yield with reference to 1-acetoxybutan-3-one is 59%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04128728
Quelldatensatzuspto-grants-1978_12
ORD IDord-6378b9e4c99d40c6811d8c8750d9496a
Quellennotizuspto-grants-1978_12