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Acetic Anhydride → N-(1-(5-Bromo-3-fluoropyridin-2-yl)vinyl)acetamide

HRID 1404563
ノート
印刷プレビュー

反応式

HRID 1404563 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([F:10])[C:5]([C:8]#[N:9])=[N:6][CH:7]=1.[CH3:11][Mg]Cl.[C:14](OC(=O)C)(=[O:16])[CH3:15]>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([F:10])[C:5]([C:8]([NH:9][C:14](=[O:16])[CH3:15])=[CH2:11])=[N:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7918Acetic AnhydrideHCID 441966805-Bromo-3-fluoropyridine-2-carbonitrileHCID 178418332HCID 178418332、化合物

生成物 1

HCID 44196681N-(1-(5-Bromo-3-fluoropyridin-2-yl)vinyl)acetamide収率 69.1%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
-10 °C

実験手順

To a solution of 5-bromo-3-fluoro-pyridine-2-carbonitrile (10 g, 49.75 mmol) in toluene (50 ml) was added MeMgCl (24.87 ml, 74.62 mmol, 3M in THF) slowly at −10° C. The reaction mixture was stirred at −10° C. for 1 h, then acetic acid anhydride (47 ml, 497.5 mmol) was added and stirring was continued for 16 h at 25° C. The reaction was then quenched by addition of saturated aqueous NaHCO3 solution (100 ml) and the resulting mixture was stirred for another 30 minutes. The organic layer was separated, washed twice with water, with brine, dried with Na2SO4 and evaporated. The remaining residue was purified by chromatography (silica gel; hexane/EtOAc 85:15-80:20) to obtain the title compound as brown solid (8.9 g, 69%).

後処理

  1. stirringstirring
  2. waitwas continued for 16 h at 25° C
  3. customThe reaction was then quenched by addition of saturated aqueous NaHCO3 solution (100 ml)
  4. stirringthe resulting mixture was stirred for another 30 minutes
  5. customThe organic layer was separated
  6. washwashed twice with water, with brine
  7. dry with materialdried with Na2SO4
  8. customevaporated
  9. customThe remaining residue was purified by chromatography (silica gel; hexane/EtOAc 85:15-80:20)

出典と根拠

ORDレコード
ord-c70d889dd28e4ce998c316a3fc6fada2
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912221B2

反応ノート

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