Potassium Hydroxide → 1-(4-Methoxy-benzyl)-3-propyl-piperidine

HRID 492647ノート

反応式

HRID 492647 の反応式
[CH3:1][O:2][C:3]1[CH:19]=[CH:18][C:6]([CH2:7][N:8]2[CH2:13][CH2:12][CH2:11][CH:10]([C:14](=O)[CH2:15][CH3:16])[CH2:9]2)=[CH:5][CH:4]=1.[OH-].[K+].O.NN.[NH4+].[Cl-]>C(O)COCCO>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[CH2:13][CH2:12][CH2:11][CH:10]([CH2:14][CH2:15][CH3:16])[CH2:9]2)=[CH:18][CH:19]=1

参加物

6

反応物 4

HCID 14797Potassium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 25517Ammonium ChlorideHCID 597303451-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-propan-1-one

生成物 1

HCID 597300471-(4-Methoxy-benzyl)-3-propyl-piperidine収率 40%

試薬・触媒・溶媒 1

HCID 8117Diethylene Glycol溶媒

反応条件

温度
120 °C

実験手順

Combine 1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-propan-1-one (277.3 mg, 1.07 mmol), Diethylene glycol (10 mL), KOH (178.0 mg, 3.18 mmol), and Hydrazine-monohydrate (1.0 mL) at room temperature under a Nitrogen atmosphere. Heat the reaction mixture to 120° C. for 2 hours and then 220° C. for 4 hours. Cool reaction to room temperature and then pour the reaction mixture over sat NH4Cl (aq). Extract with Ethyl acetate, wash with brine, and dry over Na2SO4. Concentrate under reduced pressure and flash chromatograph using 3% 1N NH3 MeOH in CH2Cl2 to give 105.2 mg (40% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 0.9 (3H, t), 1.1-1.4 (4H, m), 1.5-1.7 (3H, m), 1.7 (1H, d), 1.9 (1H, td), 2.7-2.9 (2H, m), 3.5 (2H, dd), 3.8 (3H, s), 6.8 (2H, d), 7.2 (2H, d); MS m/z 248 (M+1).

後処理

  1. customat room temperature
  2. temperatureCool
  3. customreaction to room temperature
  4. additionpour the reaction mixture
  5. extractionExtract with Ethyl acetate
  6. washwash with brine
  7. dry with materialdry over Na2SO4
  8. concentrationConcentrate under reduced pressure and flash chromatograph

出典と根拠

ORDレコード
ord-d777ed9e91214ac6bc46a320cab7d7fa
出典データセット
uspto-grants-2009_05
特許番号
US07531557B2

反応ノート

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