HCID 69352738、化合物 → HCID 69351642、化合物

HRID 1270453ノート

反応式

HRID 1270453 の反応式
C([N:8]1[CH2:13][CH2:12][CH2:11][C@H:10]([O:14][C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-])=O)=[CH:17][CH:16]=2)[CH2:9]1)C1C=CC=CC=1>CO.[Pd]>[NH2:21][C:18]1[CH:19]=[CH:20][C:15]([O:14][C@H:10]2[CH2:11][CH2:12][CH2:13][NH:8][CH2:9]2)=[CH:16][CH:17]=1

参加物

4

反応物 1

HCID 69352738HCID 69352738、化合物

生成物 1

HCID 69351642HCID 69351642、化合物収率 88%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 1-benzyl-(3S)-3-(4-nitrophenoxy)piperidine (6.5 g) and 1.2 g of 10% Pd/C in methanol (30 mL) was subjected to hydrogenation (50 psi). When the reaction was completed, the reaction mixture was filtered. The filtrate was concentrated in vacuo, giving a yellow solid. Recrystallization in CH2Cl2/hexane afforded (3S)-3-(4-aminophenoxy)piperidine (3.5 g, 88% yield) as a white solid.

後処理

  1. filtrationthe reaction mixture was filtered
  2. concentrationThe filtrate was concentrated in vacuo
  3. customgiving a yellow solid
  4. customRecrystallization in CH2Cl2/hexane

出典と根拠

ORDレコード
ord-fdf49c622e5444f698f716f7cc83b05a
出典データセット
uspto-grants-2007_04
特許番号
US07202263B2

反応ノート

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