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Hydrochloric Acid → 1-(3-Chlorophenyl)butan-1-amine

HRID 659977
ノート
印刷プレビュー

反応式

HRID 659977 の反応式
F[C:2]1[CH:3]=[C:4]([C:8](=O)[CH2:9][CH2:10][CH3:11])[CH:5]=[CH:6][CH:7]=1.C([O-])(=O)C.[NH4+:17].C([BH3-])#N.[Na+].[ClH:22]>CO>[Cl:22][C:2]1[CH:3]=[C:4]([CH:8]([NH2:17])[CH2:9][CH2:10][CH3:11])[CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 517165Ammonium AcetateHCID 5003444Sodium cyanoborohydrideHCID 204362041-(3-Fluorophenyl)butan-1-one

生成物 1

HCID 588532391-(3-Chlorophenyl)butan-1-amine収率 28%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 1-(3-fluorophenyl)butan-1-one (430 mg, 2.4 mmol) and ammonium acetate (1.09 g, 14.1 mmol) in methanol (10 mL) under nitrogen was added sodium cyanoborohydride (2.35 ml, 1M solution in THF, 2.35 mmol). The solution was stirred at room temperature for 38 h. after which time conc. HCl was added to give a pH˜2. After bubbling had ceased the solvent was removed under reduced pressure and the residue dissolved in ethyl acetate and water. The organic phase was collected and the aqueous phase washed with ethyl acetate (20 mL). The aqueous phase was basified to pH˜10 with solid KOH and the product extracted into ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried (Na2SO4) and concentrated to give a pure product (120 mg, 28%).

後処理

  1. additionwas added
  2. customto give a pH˜2
  3. customAfter bubbling
  4. customwas removed under reduced pressure
  5. dissolutionthe residue dissolved in ethyl acetate
  6. customThe organic phase was collected
  7. washthe aqueous phase washed with ethyl acetate (20 mL)
  8. extractionthe product extracted into ethyl acetate (3×20 mL)
  9. washwashed with brine
  10. dry with materialdried (Na2SO4)
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-526cc426781647b0b7e89589d9dc8680
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08084456B2

反応ノート

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