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Trifluoroacetic acid → 1-Cbz-Piperidin-4-ylidene-acetic acid

HRID 1584375
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반응식

HRID 1584375 반응식
F[C:2](F)(F)[C:3]([OH:5])=[O:4].C(OC([CH:15]1[CH2:20][CH2:19][N:18]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[C:17](=C)[CH2:16]1)=O)(C)(C)C>C(Cl)Cl>[C:3]([CH:2]=[C:15]1[CH2:20][CH2:19][N:18]([C:21]([O:23][CH2:24][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[O:22])[CH2:17][CH2:16]1)([OH:5])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 700523534-tert-butoxycarbonyl-methylene-N-CBZ-piperidine

생성물 1

HCID 212243161-Cbz-Piperidin-4-ylidene-acetic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trifluoroacetic acid (10 ml) was added to 4-tert-butoxycarbonyl-methylene-N-CBZ-piperidine (20 g, 60.3 mmol) in methylene chloride (30 ml) and the solution was stirred at room temperature for 1.5 hours. After evaporation of the solvent, the residue was triturated with diethyl ether to give 4-carboxymethylene-N-CBZ-piperidine as a crystalline white solid.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customAfter evaporation of the solvent
  • customthe residue was triturated with diethyl ether
  • 출처 및 근거

    ORD 기록
    ord-c3f956a665ca46118e18c72907f9c2cc
    출처 데이터셋
    uspto-grants-1999_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05932595

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