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Ethanol → 4-Amino-5-fluoro-2-methoxybenzoic acid

HRID 630410
ノート
印刷プレビュー

反応式

HRID 630410 の反応式
[NH2:1][C:2]1[C:9]([F:10])=[CH:8]C(C#N)=[C:4]([O:11][CH3:12])[CH:3]=1.[OH-:13].[Na+].[CH2:15]([OH:17])[CH3:16]>>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:16]([C:15]([OH:13])=[O:17])=[C:4]([O:11][CH3:12])[CH:3]=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

4

反応物 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 185196344-Amino-5-fluoro-2-methoxybenzonitrile2 回

生成物 1

HCID 674693384-Amino-5-fluoro-2-methoxybenzoic acid収率 80%

反応条件

温度
110 °C

実験手順

To a solution of 4-amino-5-fluoro-2-methoxybenzonitrile (intermediate 88; 5.3 g, 0.03 mol) in ethanol (20 mL) was added sodium hydroxide 8M (27.9 mL, 0.22 mol), the mixture was placed in a sealed vessel and heated to 110° C. for 20 hours. The solvent was removed under reduced pressure and the crude obtained was partitioned between water and ether. The aqueous layer was acidified by hydrochloric acid 6N until pH 4 and the crude was extracted with ethyl acetate, dried, filtered and evaporated under reduced pressure giving the title compound as a yellow solid (80%), which was used in the next step without further purification.

後処理

  1. customthe mixture was placed in a sealed vessel
  2. customThe solvent was removed under reduced pressure
  3. customthe crude obtained
  4. customwas partitioned between water and ether
  5. extractionthe crude was extracted with ethyl acetate
  6. customdried
  7. filtrationfiltered
  8. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-b494ab6197e44209931d40c7e221138b
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09315463B2

反応ノート

読み込み中…

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