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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 474580생성일: 2026년 10월 24일

Acetic Acid → Ethyl 2-benzyl-3-oxopropanoate

https://huagongshe.com/ko/reaction/474580

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl formateHCID 8025—
반응물Ethyl 3-phenylpropionateHCID 16237—
반응물Sodium hydrideHCID 24758—
용매1,2-DimethoxyethaneHCID 8071—
생성물Ethyl 2-benzyl-3-oxopropanoateHCID 562571100%

반응 단계

To a suspension of NaH (2.338 g, 58.5 mmol) in DME (20 mL) was added dropwise a solution of ethyl 3-phenylpropanoate (3.2 g, 19.49 mmol) and ethyl formate (6.28 mL, 78 mmol) in DME (20 mL) at room temperature. The reaction mixture was then stirred overnight. It was neutralized with acetic acid (4 mL), then extracted with EtOAc. The organic phase was collected, washed with brine, dried over Na2SO4, filtered, and concentrated affording the crude title compound (4.02 g, 100% yield). LCMS: rt=2.82 and 3.51 min (a mixture of ketone and enol isomer), [M+H+]=207.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637536B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-d27c5f8e2b6a479abcff3ee799673c13
출처 메모uspto-grants-2014_01