돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19719생성일: 2026년 10월 26일

Acetyl chloride → Methyl 2-acetyl-3-phenylbutyrate

https://huagongshe.com/reaction/19719

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물DiisopropylamineHCID 7912—
반응물Methyl 3-phenylbutanoateHCID 137945—
반응물Sodium BicarbonateHCID 516892—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-acetyl-3-phenylbutyrateHCID 12561390—

반응 단계

n-Butyllithium (2.5 M hexanes 12.4 ml, 30.9 mmol) is added to N,N-diisopropylamine (4.4 ml, 31.4 mmol) in tetrahydrofuran (THF, 50 ml) at 0° C. After 10 minutes, the resultant solution is transferred via cannula to a cooled (−78° C.) solution of methyl 3-phenylbutyrate (5.0 g, 28.05 mmol) in THF (50 ml). After 40 minutes, the resultant solution is transferred via cannula to a solution of acetyl chloride (19.15 ml) in THF (50 ml). The resultant mixture is stirred at −78° C. for 1.5 hours, then warmed to 0° C. after which water is added and the mixture is then poured into saturated NaHCO3 and extracted with EtOAc. The combined organic phases are washed with brine, dried (MgSO4) and evaporated. Purification by flash chromatography (12:1 EtOAc-hexane elution) affords the title compound. δH 1.3 (d J 7 3H), 2.3 (s 3H), 3.4 (s 3H), 3.6 (m 1H), 3.8 (m 1H), 7.2-7.4 (m 5H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745462B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f09846a5cb0b4d94b5b6987d8445cfd8
출처 메모uspto-grants-2010_06