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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1062458생성일: 2026년 10월 26일

N-bromobutanimide → Ethyl 3-cyclopropyl-2-oxopropanoate

https://huagongshe.com/reaction/1062458

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Ethyl 2-(cyclopropylmethyl)-1,3-dithiane-2-carboxylateHCID 22285400—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물Ethyl 3-cyclopropyl-2-oxopropanoateHCID 2228562955%

반응 단계

A solution of ethyl 2-(cyclopropylmethyl)-1,3-dithiane-2-carboxylate (19.6 g, 79.67 mmol) in CH3CN (20 mL) was slowly added, over 30 minutes, to a well-stirred suspension of NBS (N-bromosuccinimide) in CH3CN (210 mL) and water (55 mL). After the mixture was stirred for 1 h, the resulting red solution was poured into an ice-cold CH2Cl2-Hexane solution (1:1 500 mL). The resulting mixture was washed with saturated aqueous NaHSO3 and water. The colorless organic phase was carefully washed with saturated aqueous K2CO3 and water. The organic phase was dried over MgSO4, then evaporated to give 6.88 g (55%) of ethyl 3-cyclopropyl-2-oxopropanoate as a yellow oil. 1H NMR (CDCl3): δ 4.29 (2H, q, J=8 Hz), 2.71 (2H, d, J=9 Hz), 1.35 (3H, t, J=8 Hz), 1.05-0.98 (1H, m), 0.59-0.54 (2H, m), 0.17-0.14 (2H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960601B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-2680a0a08783459dbb5cb3df2a065150
출처 메모uspto-grants-2005_11