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

HRID 220
ノート
印刷プレビュー

反応式

HRID 220 の反応式
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
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 77922tert-Butyl carbamateHCID 1435174-Bromo-2-fluorobenzaldehyde

生成物 1

HCID 84799500tert-butyl N-(3-fluoro-4-formylphenyl)carbamate収率 97.47%

試薬・触媒・溶媒 4

HCID 10796Cesium carbonate試薬HCID 634876Binap, (A+-)-触媒
HCID 6505921
(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium
触媒
HCID 1140Toluene溶媒

反応条件

温度
100 °C

実験手順

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.

出典と根拠

ORDレコード
ord-122adeafa04f44969e42186d0dc6c6bd
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

反応ノート

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