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1-Benzyl-4-(hydroxymethyl)piperidin-4-ol → 4-(Hydroxymethyl)piperidin-4-ol

HRID 642812
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반응식

HRID 642812 반응식
C([N:8]1[CH2:13][CH2:12][C:11]([CH2:15][OH:16])([OH:14])[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>CO.[Pd]>[OH:16][CH2:15][C:11]1([OH:14])[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 140253361-Benzyl-4-(hydroxymethyl)piperidin-4-olHCID 178418361HCID 178418361, 화합물2회

생성물 1

HCID 227444734-(Hydroxymethyl)piperidin-4-ol

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A suspension of 26.0 g (117 mmol) 1-benzyl-4-hydroxymethyl-piperidin-4-ol and 5.0 g 10% Pd/C in 500 mL MeOH was hydrogenated at 50° C. and 3 bar hydrogen pressure until the theoretical hydrogen uptake had occurred (4 h). The catalyst was filtered off and washed with MeOH. After the solvent had been eliminated the residue was reacted further without purification.

후처리

  1. customwas hydrogenated at 50° C.
  2. custom(4 h)
  3. filtrationThe catalyst was filtered off
  4. washwashed with MeOH
  5. customwas reacted further without purification

출처 및 근거

ORD 기록
ord-296e78c1935344c180208533e9baa118
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07696195B2

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