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Stannous Chloride → HCID 57494449、化合物

HRID 2262652
ノート
印刷プレビュー

反応式

HRID 2262652 の反応式
[CH2:1]([N:8]1[CH2:12][CH2:11][CH:10]([C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[C:15]([O:22][CH3:23])[CH:14]=2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Sn](Cl)Cl>CO>[CH2:1]([N:8]1[CH2:12][CH2:11][CH:10]([C:13]2[CH:18]=[CH:17][C:16]([NH2:19])=[C:15]([O:22][CH3:23])[CH:14]=2)[CH2:9]1)[C:2]1[CH:3]=[CH:4][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

4

反応物 2

HCID 24479Stannous ChlorideHCID 574700891-Benzyl-3-(3-methoxy-4-nitro-phenyl)-pyrrolidine

生成物 1

HCID 57494449HCID 57494449、化合物収率 70%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

1-Benzyl-3-(3-methoxy-4-nitro-phenyl)-pyrrolidine (350 mg, 1.12 mmol) was dissolved in methanol (20 ml), tin dichloride (1.912 g, 10.08 mmol) was added, and the reaction mixture stirred at reflux for 2 h. The methanol was evaporated, 1 N sodium hydroxide (50 ml) and ethyl acetate were added and stirring continued. The tin salts were filtered off, the organic phase was separated, dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure to yield an oil (220 mg, 70%).

後処理

  1. temperatureat reflux for 2 h
  2. customThe methanol was evaporated
  3. addition1 N sodium hydroxide (50 ml) and ethyl acetate were added
  4. stirringstirring
  5. filtrationThe tin salts were filtered off
  6. customthe organic phase was separated
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. customthe solvent evaporated under reduced pressure

出典と根拠

ORDレコード
ord-41a3b2f5c24b4354a0de703e2e54918c
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07851463B2

反応ノート

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