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HRID 2231371作成日:2026年10月26日

Acetaldehyde → Ethyl 2-ethylidene-4-chloro-3-oxobutyrate

https://huagongshe.com/reaction/2231371

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物PiperidineHCID 8082—
反応物Ethyl 4-chloroacetoacetateHCID 69484—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 2-ethylidene-4-chloro-3-oxobutyrateHCID 54518096—

反応手順

0.25 part by weight of piperidine is added dropwise to a mixture of 32.9 parts by weight of ethyl 4-chloroacetoacetate and 9.6 parts by weight of acetaldehyde at -20° C. The mixture is left to stand at -20° C. for 5 to 6 hours and ice-cold 1N hydrochloric acid and ethyl acetate are then added. The ethyl acetate phase is separated off, extracted twice more with 1N hydrochloric acid and then once with water, dried over magnesium sulphate and concentrated. 35.6 parts by weight of a yellow oil are obtained, and are distilled using a bulb tube (oven temperature 80° to 110° C. under 0.07 mm). 15.5 parts by weight of product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04782162
出典データセットuspto-grants-1988_11
ORD IDord-e34ba31881ce473ead9df2b0d6453007
出典メモuspto-grants-1988_11