홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

1,4-Dibenzylpiperidin-4-ol → 4-Benzyl-4-piperidinol

HRID 1901085
노트
인쇄 미리보기

반응식

HRID 1901085 반응식
C([N:8]1[CH2:13][CH2:12][C:11]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)([OH:14])[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>[Pd].C(O)C>[CH2:15]([C:11]1([OH:14])[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 47141251,4-Dibenzylpiperidin-4-olHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 981524-Benzyl-4-piperidinol

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of N-benzyl-4-benzyl-4-piperidinol (2.0 g, 7.1 mmol) and 10% palladium on charcoal catalyst (0.5 g) in absolute ethanol (100 ml), was stirred vigorously at 40° C. under a balloon of hydrogen for 5 h. The reaction mixture was then filtered through a pad of Celite and the filtrate concentrated in vacuo to a grayish solid. This material was dissolved in methanol and filtered a second time through Celite and the filtrate concentrated in vacuo to the product, a white solid.

후처리

  1. filtrationThe reaction mixture was then filtered through a pad of Celite
  2. concentrationthe filtrate concentrated in vacuo to a grayish solid
  3. dissolutionThis material was dissolved in methanol
  4. filtrationfiltered a second time through Celite
  5. concentrationthe filtrate concentrated in vacuo to the product

출처 및 근거

ORD 기록
ord-b57c6caebf254421a1e6d52301a68676
출처 데이터셋
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05576313

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트