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Ethyl Acetate → HCID 14370871、化合物

HRID 1199602
ノート
印刷プレビュー

反応式

HRID 1199602 の反応式
[F:1][C:2]1[CH:8]=[C:7]([Br:9])[C:6]([O:10][C:11]([O:13][CH3:14])=[O:12])=[CH:5][C:3]=1[NH2:4].[C:15](OCC)(=[O:17])C>>[F:1][C:2]1[CH:8]=[C:7]([Br:9])[C:6]([O:10][C:11]([O:13][CH3:14])=[O:12])=[CH:5][C:3]=1[N:4]=[C:15]=[O:17]
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

3

反応物 2

HCID 8857Ethyl Acetate2 回HCID 14370869HCID 14370869、化合物

生成物 1

HCID 14370871HCID 14370871、化合物収率 94%

反応条件

温度
80 °C

実験手順

A solution of trichloromethyl chloroformate trichloromethyl (15 ml, 125 mmol) in ethyl acetate was charged into a 500 ml-three neck flask equipped with a dropping funnel and distillation apparatus and, a solution of 2-fluoro-4-bromo-5-methoxycarbonyloxyaniline (28.0 g,113 mmol) in ethyl acetate (100 ml) was added dropwise over 20 minutes. After dropping, the mixture was heated at 80° C. and ethyl acetate was removed by distillation. After cooling, carbon tetrachloride (150 ml) was added and the undissolved substances were removed by filtration. The solvent was then removed from the filtrate by distillation under reduced pressure, whereby a brown solid of 2-fluoro-4-bromo-5-methoxycarbonyloxyphenyl isocyanate (29.1 g, yield 94%) was obtained.

後処理

  1. customequipped with a dropping funnel
  2. distillationdistillation apparatus
  3. customethyl acetate was removed by distillation
  4. temperatureAfter cooling
  5. additioncarbon tetrachloride (150 ml) was added
  6. customthe undissolved substances were removed by filtration

出典と根拠

ORDレコード
ord-6b8ccc9400fa4e49b92fb48100c5052e
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04902337

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート