Acetic Acid → N-(2-(3-Chlorophenyl)ethyl)-3-benzoylbenzylamine

HRID 1666825ノート

反応式

HRID 1666825 の反応式
[C:1]([C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH:12]=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:17][C:18]1[CH:19]=[C:20]([CH2:24][CH2:25][NH2:26])[CH:21]=[CH:22][CH:23]=1.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>CO.ClC(Cl)C.CCOC(C)=O>[Cl:17][C:18]1[CH:19]=[C:20]([CH2:24][CH2:25][NH:26][CH2:12][C:11]2[CH:14]=[CH:15][CH:16]=[C:9]([C:1](=[O:8])[C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH:10]=2)[CH:21]=[CH:22][CH:23]=1

参加物

8

実験手順

Combine 3-benzoylbenzaldehyde (0.45 g, 2.1 mmol), and (3-chlorophenyl)ethylamine (0.3 ml, 2.1 mmol) and 3 Å molecular sieves (1.0 g) in MeOH (30 ml). Heat to reflux. After 3 hours, cool, filter, and concentrate to give a residue. Dissolve the residue in dichloroethane (20 ml), add acetic acid (0.12 ml, 2.1 mmol) and sodium triacetoxyborohydride (0.6 g, 2.94 mmol) and stir at ambient temperature. After 2 hours, concentrate the reaction mixture and add dichloromethane (90 ml) and extract sequentially with distilled water (50 ml) and then brine (50 ml). Dry the organic layer over Na2SO4 and give a residue. Chromatograph the residue on silica gel eluting with EtOAc to give the title compound as the base.

後処理

  1. temperatureHeat to reflux
  2. temperaturecool
  3. filtrationfilter
  4. concentrationconcentrate
  5. customto give a residue
  6. waitAfter 2 hours
  7. concentrationconcentrate the reaction mixture
  8. additionadd dichloromethane (90 ml)
  9. extractionextract sequentially with distilled water (50 ml)
  10. dry with materialDry the organic layer over Na2SO4
  11. customgive a residue

出典と根拠

ORDレコード
ord-f1da5b5d94024389bfb2fe6e434a48de
出典データセット
uspto-grants-2011_10
特許番号
US08044090B2

反応ノート

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