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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221970생성일: 2026년 10월 27일

3-Chloro-2-chloromethyl-1-propene → Ethyl 2-(4-bromophenyl)-4-(chloromethyl)pent-4-enoate

https://huagongshe.com/reaction/221970

반응식

참여 물질

역할이름HCID투입량
반응물3-Chloro-2-chloromethyl-1-propeneHCID 15859—
반응물Sodium BicarbonateHCID 516892—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물Ethyl 2-(4-bromophenyl)acetateHCID 7020609—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-(4-bromophenyl)-4-(chloromethyl)pent-4-enoateHCID 59161543—

반응 단계

To a solution of ethyl (4-bromophenyl)acetate (143 g, 588 mmol) in THF (800 mL) was added LHMDS (1.13 eq in THF) at −78° C. After 30 minutes, the reaction mixture was added to a solution of 3-chloro-2-chloromethyl-1-propene (147 g, 1180 mmol) in THF (500 mL) at −78° C. via cannula. The reaction was allowed to slowly warm from −78° C. to rt over 15 hours. The reaction mixture was poured into sodium bicarbonate, extracted with EtOAc, dried over sodium sulfate, filtered and concentrated. The crude residue was purified by column chromatography eluting with 1-20% EtOAc/Hexane. The appropriate fractions were combined and the solvent removed in vacuo to give ethyl 2-(4-bromophenyl)-4-(chloromethyl)pent-4-enoate (1-1) as a clear oil. MS (M+H)+: 332.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207169B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-2fe2a5c6810a4b97933ac6b5f2bffc25
출처 메모uspto-grants-2012_06