Hydrogen Peroxide → 4-Methoxy-3-phenylphenethylamine

HRID 440541ノート

反応式

HRID 440541 の反応式
Br.Br[C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[CH2:6][CH2:7][NH2:8].C(=O)([O-])[O-].[Na+].[Na+].[C:20]1(OB(O)O)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.OO>C(O)C.C1(C)C=CC=CC=1>[CH3:13][O:12][C:11]1[CH:10]=[CH:9][C:5]([CH2:6][CH2:7][NH2:8])=[CH:4][C:3]=1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

参加物

7

反応物 4

HCID 784Hydrogen PeroxideHCID 10340Sodium CarbonateHCID 78412Phenyl dihydrogen orthoborateHCID 224068232-(3-Bromo-4-methoxyphenyl)ethan-1-amine hydrobromide

生成物 1

HCID 224068554-Methoxy-3-phenylphenethylamine

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 1140Toluene溶媒

実験手順

A mixture of tetrakis triphenylphosphine palladium (7 g), 3-bromo-4-methoxyphenethylamine hydrobromide (62.2 g) and toluene (400 ml) was stirred under nitrogen with 2M aqueous sodium carbonate solution (200 ml) and then a solution of phenyl boric acid (26.8 g) in ethanol (100 ml) was added. The mixture was heated under reflux for 48 hours then cooled and treated with 30% aqueous hydrogen peroxide solution (10 ml). The mixture was stirred at ambient temperature for 1 hour. The aqueous layer was separated and extracted with ether. The ether extracts were combined with the original organic phase. Distillation yielded 4-methoxy-3-phenylphenethylamine which was used without further purification.

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 48 hours
  3. temperaturethen cooled
  4. customThe aqueous layer was separated
  5. extractionextracted with ether
  6. distillationDistillation

出典と根拠

ORDレコード
ord-c173b890f7c14b75bdfa64d4eadcdfd0
出典データセット
uspto-grants-1996_05
特許番号
US05519034

反応ノート

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