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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219생성일: 2026년 10월 23일

tert-Butyl carbamate → tert-butyl N-(3-fluoro-4-formylphenyl)carbamate

https://huagongshe.com/ko/reaction/219

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참여 물질

역할이름HCID투입량
반응물tert-Butyl carbamateHCID 77922—
반응물4-Bromo-2-fluorobenzaldehydeHCID 143517—
시약Cesium carbonateHCID 10796—
촉매Binap, (A+-)-HCID 634876—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매TolueneHCID 1140—
생성물tert-butyl N-(3-fluoro-4-formylphenyl)carbamateHCID 8479950083.59%

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온도100 °C

반응 단계

A solution of 4-bromo-2-fluorobenzaldehyde (0.670 g, 3.30 mmol) dissolved in toluene (10 mL) was treated with tert-butyl carbamate (0.464 g, 3.96 mmol), rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.164 g, 0.26 mmol), Bis(dibenzylideneacetone)palladium (0.076 g, 0.13 mmol) and cesium carbonate (1.527 g, 4.69 mmol) under nitrogen. The mixture was degassed under vacuum several times before heating at 100 °C for 24 hours. Reaction incomplete so heated for further 10 hours. The reaction mixture was diluted with water (250 mL), and extracted with ethyl acetate (250 mL X 2). The organic was dried over magnesium sulfate, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution 10% ethyl acetate in isohexane. Pure fractions were evaporated to dryness to afford tert-butyl 3-fluoro-4-formylphenylcarbamate (0.660 g, 84 %) as a yellow solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-41642501237541609124229452d981cb
출처 메모750 AstraZeneca ELN dataset