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Trifluoroacetic acid → HCID 131711089, 화합물

HRID 2083836
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HRID 2083836 반응식
C(OC([NH:8][C@H:9]([C:19]([OH:21])=[O:20])[CH2:10][O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=O)(C)(C)C.[F:22][C:23]([F:28])([F:27])[C:24]([OH:26])=[O:25]>>[F:22][C:23]([F:28])([F:27])[C:24]([OH:26])=[O:25].[CH2:12]([O:11][CH2:10][C@@H:9]([C:19]([OH:21])=[O:20])[NH2:8])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 90234L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-

생성물 1

HCID 131711089HCID 131711089, 화합물

실험 절차

Nα -t-Butoxycarbonyl-O-benzyl-L-serine, 5.0 g., is treated with 20 ml. of trifluoroacetic acid at 5° C. The solution is let stand at room temperature for 15 minutes and then the excess trifluoroacetic acid removed under reduced pressure. Benzene is added followed by evaporation. This process is repeated three times to remove excess trifluoroacetic acid. Finally the product is dried under reduced pressure and used without further treatment.

후처리

  1. addition, is treated with 20 ml
  2. customat 5° C
  3. customat room temperature
  4. customfor 15 minutes
  5. customthe excess trifluoroacetic acid removed under reduced pressure
  • additionBenzene is added
  • customfollowed by evaporation
  • customto remove excess trifluoroacetic acid
  • customFinally the product is dried under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-dbf16c0531f441ba93bc10686782bc53
    출처 데이터셋
    uspto-grants-1978_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04086219

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