N-((1-Benzylpyrrolidin-3-yl)methyl)propan-2-amine → N-(Pyrrolidin-3-ylmethyl)propan-2-amine

HRID 364045ノート

反応式

HRID 364045 の反応式
C1(C[N:8]2[CH2:12][CH2:11][CH:10]([CH2:13][NH:14][CH:15]([CH3:17])[CH3:16])[CH2:9]2)C=CC=CC=1.[H][H]>[Pd].CO>[CH3:16][CH:15]([NH:14][CH2:13][CH:10]1[CH2:11][CH2:12][NH:8][CH2:9]1)[CH3:17]

参加物

5

反応物 2

HCID 14280887N-((1-Benzylpyrrolidin-3-yl)methyl)propan-2-amineHCID 178418361HCID 178418361、化合物

生成物 1

HCID 13491802N-(Pyrrolidin-3-ylmethyl)propan-2-amine収率 76.4%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 13.4 g (58.0 mmol) of 1-phenylmethyl-N-(2-propyl)-3-pyrrolidinemethanamine, 1.0 g of 20% palladium on carbon and 130 ml of methanol was shaken in an atmosphere of hydrogen at about 50 psi and room temperature for 24 hours. The catalyst was removed by filtration through Celite; the filtrate concentrated and distilled in vacuo to give 6.3 g of N-(2-propyl)-3-pyrrolidinemethanamine, bp 58°-60° C./3.5 mm.

後処理

  1. customThe catalyst was removed by filtration through Celite
  2. concentrationthe filtrate concentrated
  3. distillationdistilled in vacuo

出典と根拠

ORDレコード
ord-7bbc8b96be0d4768a278540ac6403506
出典データセット
uspto-grants-1986_08
特許番号
US04604401

反応ノート

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