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Acetic Acid → N-[4-amino-2-fluoro-5-(2-hydroxyphenoxy)phenyl]acetamide

HRID 1280374
ノート
印刷プレビュー

反応式

HRID 1280374 の反応式
C(O)(=O)C.[F:5][C:6]1[CH:11]=[C:10]([N+:12]([O-])=O)[C:9]([O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[OH:22])=[CH:8][C:7]=1[NH:23][C:24](=[O:26])[CH3:25].C(OCC)(=O)C>[Fe].O>[NH2:12][C:10]1[C:9]([O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[OH:22])=[CH:8][C:7]([NH:23][C:24](=[O:26])[CH3:25])=[C:6]([F:5])[CH:11]=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

6

反応物 3

HCID 176Acetic AcidHCID 8857Ethyl AcetateHCID 21933568N-[2-fluoro-5-(2-hydroxyphenoxy)-4-nitrophenyl]acetamide

生成物 1

HCID 18759282N-[4-amino-2-fluoro-5-(2-hydroxyphenoxy)phenyl]acetamide収率 82.3%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 962Water
溶媒
2 回

反応条件

温度
80 °C

実験手順

Into a mixture of 25 ml of acetic acid and 25 ml of water was added 9.5 g of an iron powder, and the mixture was heated to 80° C. Into the mixture was added dropwise a solution composed of 10.0 g of N-[2-fluoro-5-(2-hydroxyphenoxy)-4-nitrophenyl]acetamide and 100 ml of ethyl acetate. The mixture was heated for 1 hour under reflux, then, poured into water, extracted with ethyl acetate, the organic layer was washed with water, and washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated to obtain 7.42 g of N-[4-amino-2-fluoro-5-(2-hydroxyphenoxy)phenyl]acetamide.

後処理

  1. additionInto the mixture was added dropwise a solution
  2. temperatureThe mixture was heated for 1 hour
  3. temperatureunder reflux
  4. extractionextracted with ethyl acetate
  5. washthe organic layer was washed with water
  6. washwashed with saturated aqueous sodium bicarbonate
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-56bbd5674eec44f58e9a58cded7465e8
出典データセット
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06451740B2

反応ノート

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