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1-Benzyloxycarbonyl-4-(4-hexyloxyphenyl)-4-hydroxypiperidine → 4-[4-(Hexyloxy)phenyl]piperidin-4-OL

HRID 351544
노트
인쇄 미리보기

반응식

HRID 351544 반응식
C(OC([N:11]1[CH2:16][CH2:15][C:14]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[CH:20][CH:19]=2)([OH:17])[CH2:13][CH2:12]1)=O)C1C=CC=CC=1>CO>[CH2:25]([O:24][C:21]1[CH:22]=[CH:23][C:18]([C:14]2([OH:17])[CH2:13][CH2:12][NH:11][CH2:16][CH2:15]2)=[CH:19][CH:20]=1)[CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 227131741-Benzyloxycarbonyl-4-(4-hexyloxyphenyl)-4-hydroxypiperidine

생성물 1

HCID 227132354-[4-(Hexyloxy)phenyl]piperidin-4-OL수율 78.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 1-benzyloxycarbonyl-4-(4-hexyloxyphenyl)-4-hydroxypiperidine (1.4 g) in methanol (28 ml) was added dry 10% palladium on carbon (0.7 g) and stirred for 6 hours under hydrogen atmosphere. The palladium on carbon was filtered off, and the filtrate was evaporated under reduced pressure to give 4-(4-hexyloxyphenyl)-4-hydroxypiperidine (0.74 g).

후처리

  1. dry with materialdry 10% palladium on carbon (0.7 g)
  2. filtrationThe palladium on carbon was filtered off
  • customthe filtrate was evaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-650922ac70674b5c8def7a80bdb34c6c
    출처 데이터셋
    uspto-grants-2004_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06743776B2

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