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Water → HCID 21252689, 화합물

HRID 1530800
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HRID 1530800 반응식
[F:1][C:2]([F:13])([F:12])[CH2:3][CH2:4][CH:5]1[CH2:10][CH2:9][CH:8]([OH:11])[CH2:7][CH2:6]1.O.CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.C(=O)([O-])O.[Na+]>CC(C)=O.C(O)(C)C>[F:1][C:2]([F:12])([F:13])[CH2:3][CH2:4][CH:5]1[CH2:10][CH2:9][C:8](=[O:11])[CH2:7][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 516892Sodium BicarbonateHCID 21252690HCID 21252690, 화합물HCID 131709961Jones' reagent

생성물 1

HCID 21252689HCID 21252689, 화합물

시약·촉매·용매 2

HCID 180Acetone용매HCID 3776
Isopropanol
용매

실험 절차

35.6 g of 4-(3,3,3-trifluoropropyl)cyclohexanol were dissolved in 600 ml of acetone and 37 ml of water and mixed with 69 ml of Jones reagent. The mixture was stirred at room temperature for 24 h, mixed with 9 ml of isopropanol and 24 g of sodium hydrogen carbonate, the precipitate was filtered off and the residue was taken up in saturated aqueous sodium chloride. The mixture was extracted with ether and the combined ether phases were washed with water, dried and concentrated. Chromatography over silica gel (petroleum ether/ethyl acetate=3:1) gave the title product as a colourless oil.

후처리

  1. filtrationthe precipitate was filtered off
  2. extractionThe mixture was extracted with ether
  3. washthe combined ether phases were washed with water
  4. customdried
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-92ab901a5dbc4df1b779a4bcb638b5bc
출처 데이터셋
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06197729B1

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