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Triacetoxyperiodinane → HCID 59540695, 화합물

HRID 1677409
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HRID 1677409 반응식
[F:1][C:2]([F:12])([F:11])[C:3]([CH3:10])([C:6]([F:9])([F:8])[F:7])[CH2:4][OH:5].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>>[F:1][C:2]([F:11])([F:12])[C:3]([CH3:10])([C:6]([F:7])([F:9])[F:8])[CH:4]=[O:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 159087TriacetoxyperiodinaneHCID 27361853,3,3-Trifluoro-2-methyl-2-(trifluoromethyl)propan-1-ol

생성물 1

HCID 59540695HCID 59540695, 화합물

반응 조건

온도
100 °C

실험 절차

3,3,3-Trifluoro-2-methyl-2-trifluoromethyl-propan-1-ol, 1 gm, 5.1 mM, and Dess-Martin Periodinane, 4.3 gm, 10.2 mM, 2 eq. was added to ten ml of 1,1,1,3 tetrachloroethane and the mixture stirred for several hours. A short path distillation head was added and the receiver flask was cooled in dry ice-acetone bath. The mixture was heated to 100° C. and the pressure lowered to 180 Ton. The desired product 3,3,3-Trifluoro-2-methyl-2-trifluoromethyl-propionaldehyde condensed in the receiver flask and was used without further purification in the above reaction.

후처리

  1. distillation
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
A short path distillation head
  • additionwas added
  • temperaturethe receiver flask was cooled in dry ice-acetone bath
  • customThe desired product 3,3,3-Trifluoro-2-methyl-2-trifluoromethyl-propionaldehyde condensed in the receiver flask
  • customwas used without further purification in the above reaction
  • 출처 및 근거

    ORD 기록
    ord-e704309765e7428b8be03d1f1c6a7df3
    출처 데이터셋
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08008298B2

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