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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Chloro-2-chloromethyl-1-propene | HCID 15859 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | Ethyl 2-(4-bromophenyl)acetate | HCID 7020609 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 2-(4-bromophenyl)-4-(chloromethyl)pent-4-enoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08207169B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-2fe2a5c6810a4b97933ac6b5f2bffc25 |
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| 출처 메모 | uspto-grants-2012_06 |
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