Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384072생성일: 2026년 10월 24일
Phosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1) → methyl (E)-3-[3-bromo-5-(1-cyanocyclopropyl)phenyl]prop-2-enoate
https://huagongshe.com/ko/reaction/384072
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1) | HCID 2733211 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | HCID 57969743 | HCID 57969743 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | methyl (E)-3-[3-bromo-5-(1-cyanocyclopropyl)phenyl]prop-2-enoate | HCID 86636473 | 97.1% |
반응 단계
To a suspension of (2-methoxy-2-oxo-ethyl)-triphenyl-phosphonium bromide (1.502 g, 3.618 mmol) in THF (15 mL) under nitrogen at room temperature was added LHMDS in THF (3.358 mL of 1 M, 3.358 mmol) dropwise. The mixture was stirred for 10 mins then cooled to −25° C. 1-(3-bromo-5-formyl-phenyl)cyclopropane-1-carbonitrile (500 mg, 1.999 mmol) was dissolved in 1 mL of THF and added to the reaction. The reaction was allowed to warm to room temperature over 1 hour. The reaction was quenched with MeOH (2 mL) and then partitioned between ethyl acetate and brine. The aqueous was extracted with ethyl acetate and dried, filtered and concentrated. The crude product was purified on silica (Companion, 24 g) eluting with 1-20% EtOAc:Petrol ether to give methyl (E)-3-[3-bromo-5-(1-cyanocyclopropyl)phenyl]prop-2-enoate as a yellow solid (594 mg, 97%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08367697B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-7cee1abc5af14b87a6eed0dc1efcdd95 |
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| 출처 메모 | uspto-grants-2013_02 |
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