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Acetic Acid → 4-(4-Fluoro-benzyl)-piperidin-4-ol acetate

HRID 854605
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인쇄 미리보기

반응식

HRID 854605 반응식
C([N:8]1[CH2:13][CH2:12][C:11]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)([OH:14])[CH2:10][CH2:9]1)C1C=CC=CC=1.[C:23](O)(=[O:25])[CH3:24]>C(O)C.[Pd]>[C:23]([O:14][C:11]1([CH2:15][C:16]2[CH:17]=[CH:18][C:19]([F:22])=[CH:20][CH:21]=2)[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1)(=[O:25])[CH3:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 108280121-Benzyl-4-(4-fluoro-benzyl)-piperidin-4-ol

생성물 1

HCID 694266924-(4-Fluoro-benzyl)-piperidin-4-ol acetate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of 1-benzyl-4-(4-fluoro-benzyl)-piperidin-4-ol (5.87 g, 19.6 mmol) in ethanol (80 ml) is treated with acetic acid (1 ml) and with 10% Pd on carbon (1 g). The mixture is stirred at RT under an atmosphere of hydrogen for 20 hours. The mixtre is filtered and the filtrate evaporated. The crude product is treated with dichloromethane. The resultant suspension is filtered and the white solid obtained is washed with cold dichloromethane to afford 4-(4-fluoro-benzyl)-piperidin-4-ol acetate [MH]+ 210.1

후처리

  1. filtrationThe mixtre is filtered
  2. customthe filtrate evaporated
  3. additionThe crude product is treated with dichloromethane
  4. filtrationThe resultant suspension is filtered
  5. customthe white solid obtained
  6. washis washed with cold dichloromethane

출처 및 근거

ORD 기록
ord-8b0391816e4e46d2bdd4ac7b476dd644
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07259173B2

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