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

HRID 220

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HRID 220 반응식
CC(C)(C)OC(N)=O.O=Cc1ccc(Br)cc1F>Cc1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C(/C=C/c1ccccc1)/C=C/c1ccccc1.O=C([O-])[O-].[Cs+].[Cs+].[Pd].c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1>CC(C)(C)OC(=O)Nc1ccc(C=O)c(F)c1

참가 물질

7

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온도
100 °C

실험 절차

A solution of 4-bromo-2-fluorobenzaldehyde (3.09 g, 15.22 mmol) dissolved in toluene (40 mL) was treated with tert-butyl carbamate (2.140 g, 18.27 mmol), rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.758 g, 1.22 mmol), Bis(dibenzylideneacetone)palladium (0.350 g, 0.61 mmol) and cesium carbonate (7.04 g, 21.62 mmol) under nitrogen. The mixture was degassed under vacuum several times before heating at 100 °C for 30 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 (3.55 g, 97 %) as a yellow solid.

출처 및 근거

ORD 기록
ord-122adeafa04f44969e42186d0dc6c6bd
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
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