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(1,4-Dibenzylpiperazin-2-yl)-N,N-dimethylmethanamine → N,N-dimethyl-2-piperazinemethanamine

HRID 2165601
ノート
印刷プレビュー

反応式

HRID 2165601 の反応式
[CH3:1][N:2]([CH2:4][CH:5]1[CH2:10][N:9](CC2C=CC=CC=2)[CH2:8][CH2:7][N:6]1CC1C=CC=CC=1)[CH3:3]>C(O)C.C1CCCCC1.C(O)(=O)C.[Pd]>[CH3:1][N:2]([CH3:3])[CH2:4][CH:5]1[CH2:10][NH:9][CH2:8][CH2:7][NH:6]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 1

HCID 14664170(1,4-Dibenzylpiperazin-2-yl)-N,N-dimethylmethanamine

生成物 1

HCID 14664185N,N-dimethyl-2-piperazinemethanamine

試薬・触媒・溶媒 4

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒HCID 702Ethanol溶媒HCID 8078Cyclohexane溶媒

実験手順

このページの内容参加物実験手順後処理出典と根拠反応ノート

A 4.7 g portion of 2-dimethylaminomethyl-1,4-bis(phenylmethyl)piperazine was dissolved in a mixture of 50 ml of ethanol, 20 ml of cyclohexane and 10 ml of glacial acetic acid. A 2.0 g portion of 10% palladium on carbon was added, the mixture was refluxed overnight and then filtered. The filtrate was evaporated, 5 ml of saturated aqueous potassium bicarbonate was added to the residue and this was extracted several times with dichloromethane. The extracts were combined, dried, filtered and evaporated, giving a gum which solidified on standing, giving 1.02 g of N,N-dimethyl-2-piperazinemethanamine.

後処理

  1. temperaturethe mixture was refluxed overnight
  2. filtrationfiltered
  3. customThe filtrate was evaporated
  4. addition5 ml of saturated aqueous potassium bicarbonate was added to the residue
  5. extractionthis was extracted several times with dichloromethane
  6. customdried
  7. filtrationfiltered
  8. customevaporated
  9. customgiving a gum which

出典と根拠

ORDレコード
ord-a9bba0b092ec4bc699d1e52a3d9aeb93
出典データセット
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04940710

反応ノート

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