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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1920860생성일: 2026년 10월 25일

Phosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1) → methyl (E)-3-[3-bromo-5-(1-cyanocyclopropyl)phenyl]prop-2-enoate

https://huagongshe.com/reaction/1920860

반응식

참여 물질

역할이름HCID투입량
반응물Phosphonium, (2-methoxy-2-oxoethyl)triphenyl-, bromide (1:1)HCID 2733211—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물HCID 57969743HCID 57969743—
용매TetrahydrofuranHCID 8028—
생성물methyl (E)-3-[3-bromo-5-(1-cyanocyclopropyl)phenyl]prop-2-enoateHCID 8663647397.1%

반응 조건

온도-25 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08173635B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-65b330ad44924c08be48c7f91ca5f2d5
출처 메모uspto-grants-2012_05