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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1947240생성일: 2026년 10월 27일

Acetic Acid → 4-(2-Acetyl-3-oxo-1-butenyl)benzonitrile

https://huagongshe.com/reaction/1947240

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PiperidineHCID 8082—
반응물AcetylacetoneHCID 31261—
반응물4-CyanobenzaldehydeHCID 66042—
용매DichloromethaneHCID 6344—
생성물4-(2-Acetyl-3-oxo-1-butenyl)benzonitrileHCID 367453—

반응 단계

2.3 g (17.5 mmol) of 4-formylbenzonitrile, 1.98 ml (19.29 mmol) of 2,4-pentanedione, 1 ml (26 mmol) of acetic acid and 0.34 ml (3.5 mmol) of piperidine in 40 ml of anhydrous dichloromethane are stirred under reflux with a water trap for 24 h. After cooling, the reaction solution is washed successively with saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and concentrated. The residue is recrystallized from diethyl ether. 3.18 g (85% of theory) of the title compound are obtained as a pale brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399471B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-45ed79f9ee9e4308ae54dab9054494e2
출처 메모uspto-grants-2013_03