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HRID 65808作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Acetyloxy)-2-butanoneHCID 139100—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
生成物2,3,6-Trimethylcyclohex-2-en-1-oneHCID 3016843—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04128728
出典データセットuspto-grants-1978_12
ORD IDord-6378b9e4c99d40c6811d8c8750d9496a
出典メモuspto-grants-1978_12