Methanol → 2-Amino-5-chloro-alpha-(2-fluorophenyl)benzenemethanol

HRID 358037

反応式

HRID 358037 の反応式
[BH4-].[Na+].[NH2:3][C:4]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:5]=1[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[F:14])=[O:7].CO>O>[NH2:3][C:4]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:5]=1[CH:6]([OH:7])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[F:14]

参加物

5

反応物 3

HCID 887MethanolHCID 699122-Amino-5-chloro-2'-fluorobenzophenoneHCID 4311764Sodium borohydride

生成物 1

HCID 129000332-Amino-5-chloro-alpha-(2-fluorophenyl)benzenemethanol

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of 18.5 g of sodium borohydride in 125 ml of water is added dropwise at 20° to 25° within 20 minutes to a solution of 124.8 g of 2-amino-5-chloro-2'-fluorobenzophenone. The mixture is stirred for a further 16 hours. 250 ml of methanol are then added thereto and the mixture is heated to boiling under reflux for 15 minutes. After evaporation of the organic solvent, the residue is diluted with water, whereupon the mixture is acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate solutions are washed, dried, concentrated to 100 ml in vacuo and subsequently treated with 300 ml of petroleum ether. There is obtained crystalline 2-amino-5-chloro-2'-fluorobenzhydrol of melting point 97°-99°.

後処理

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 15 minutes
  3. customAfter evaporation of the organic solvent
  4. additionthe residue is diluted with water, whereupon the mixture
  5. extractionextracted with ethyl acetate
  6. washThe ethyl acetate solutions are washed
  7. customdried
  8. concentrationconcentrated to 100 ml in vacuo
  9. additionsubsequently treated with 300 ml of petroleum ether

出典と根拠

ORDレコード
ord-6220c8076f4942249ef37c1b7e364337
出典データセット
uspto-grants-1984_08
特許番号
US04464300

関連ノート

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