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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2231371생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2231371

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물PiperidineHCID 8082—
반응물Ethyl 4-chloroacetoacetateHCID 69484—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-ethylidene-4-chloro-3-oxobutyrateHCID 54518096—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04782162
출처 데이터셋uspto-grants-1988_11
ORD IDord-e34ba31881ce473ead9df2b0d6453007
출처 메모uspto-grants-1988_11