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Triphenylphosphine → (s)-1-(3-Nitrophenyl)ethanamine

HRID 1255823
ノート
印刷プレビュー

反応式

HRID 1255823 の反応式
[N:1]([C@H:4]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1)[CH3:5])=[N+]=[N-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C1(C)C=CC=CC=1.O.C(OCC)(=O)C>[N+:12]([C:8]1[CH:7]=[C:6]([C@@H:4]([NH2:1])[CH3:5])[CH:11]=[CH:10][CH:9]=1)([O-:14])=[O:13]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 11776TriphenylphosphineHCID 866418551-[(1S)-1-azidoethyl]-3-nitrobenzene

生成物 1

HCID 11292459(s)-1-(3-Nitrophenyl)ethanamine収率 92%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 1140Toluene溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

To a solution of 1-[(1S)-1-azidoethyl]-3-nitrobenzene (16.5 g, 86 mmol) in a mixture of toluene (325 mL) and water (40 mL) was added triphenylphosphine (44.5 g, 170 mmol) in one portion. The mixture was immediately heated to 80° C. where it was stirred for 3 hours. After this time the mixture was allowed to cool to room temperature, was diluted with ethyl acetate (100 mL), the two phases separated and the organic phase extracted with dilute aqueous hydrochloric acid (2M, 3×100 mL). The acidic extracts were basified to pH>10 with solid potassium hydroxide and were then extracted with dichloromethane (3×100 mL). The organic extracts were washed with brine (100 mL), dried (MgSO4) and concentrated under reduced pressure to give (1S)-1-(3-nitrophenyl)ethanamine (13.1 g, 92%) as a yellow liquid.

後処理

  1. temperatureto cool to room temperature
  2. customthe two phases separated
  3. extractionthe organic phase extracted with dilute aqueous hydrochloric acid (2M, 3×100 mL)
  4. extractionwere then extracted with dichloromethane (3×100 mL)
  5. washThe organic extracts were washed with brine (100 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-f58733995c724d5f9552557869f9c78f
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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