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Hydrochloric Acid → 1-(3-Bromophenyl)ethanamine

HRID 1255832
ノート
印刷プレビュー

反応式

HRID 1255832 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([C:8](=O)[CH3:9])[CH:5]=[CH:6][CH:7]=1.C([O-])=O.[NH4+:14].Cl>CO.O.C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]1[C](C)[C](C)[C](C)[C]1C.Cl[Rh]Cl.Cl[Rh]Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([NH2:14])[CH3:9])[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

7

反応物 3

HCID 313Hydrochloric AcidHCID 165023'-BromoacetophenoneHCID 2723923Ammonium formate

生成物 1

HCID 167857641-(3-Bromophenyl)ethanamine収率 85%

試薬・触媒・溶媒 3

HCID 16212157Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]触媒HCID 887
Methanol
溶媒
HCID 962Water溶媒

実験手順

A mixture of 3′-bromoacetophenone (2.66 mL, 20 mmol), ammonium formate (6.31 g, 100 mmol) and dichloro(pentamethylcyclopentadienyl)rhodium(III) dimer (124 mg, 0.2 mmol) in anhydrous methanol (20 mL) under an atmosphere of nitrogen was heated at reflux for 5 hours then allowed to cool to room temperature overnight. The mixture was diluted with water (20 mL), acidified to pH 2 with dilute aqueous hydrochloric acid (2M) and washed with dichloromethane (2×60 mL). The aqueous solution was basified to pH 12 with solid potassium hydroxide, extracted with dichloromethane (3×50 mL) and the extracts washed with brine (50 mL), dried (Na2SO4) and concentrated under reduced pressure to give 1-(3-bromophenyl)ethanamine (3.4 mg, 85%) as a yellow liquid.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 5 hours
  3. washwashed with dichloromethane (2×60 mL)
  4. extractionextracted with dichloromethane (3×50 mL)
  5. washthe extracts washed with brine (50 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-0f2c8b8abbd44aa49c644c9fcf7dadab
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08461161B2

反応ノート

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