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Pivaloyl chloride → 4-(4-Chlorobenzoyl)phenyl 2,2-dimethylpropanoate

HRID 2292185
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HRID 2292185 반응식
[OH:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.[C:17](Cl)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]>N1C=CC=CC=1>[C:17]([O:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 62493Pivaloyl chlorideHCID 1235044-Hydroxy-4'-chlorobenzophenone

생성물 1

HCID 140104074-(4-Chlorobenzoyl)phenyl 2,2-dimethylpropanoate

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

2.16 g (0.01 mole) of 4-hydroxy-4'-chlorobenzophenone and 1.2 g (0.015 mole) of pivaloyl chloride in solution were warmed to 50° C. for 3 hrs in 60 mls of dry pyridine with a drying tube attached. The solvent was removed via rotary evaporator and H2O added. The product was filtered and recrystallized from ethanol; 2.3 g (73%) yield; M.P.~113°-114° C.

후처리

  • customThe solvent was removed via rotary evaporator and H2O
  • additionadded
  • filtrationThe product was filtered
  • customrecrystallized from ethanol
  • custom2.3 g (73%) yield
  • 출처 및 근거

    ORD 기록
    ord-39173646bd3e4f2d88afaa486cc59188
    출처 데이터셋
    uspto-grants-1989_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04801610

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