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

HRID 248456
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HRID 248456 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 1

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

생성물 1

HCID 14664185N,N-dimethyl-2-piperazinemethanamine

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 176Acetic Acid용매HCID 702Ethanol용매HCID 8078Cyclohexane용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f962c2fba81642c2a6d4365241e98f34
출처 데이터셋
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05210193

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