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2,2-Difluorocyclopropyl(4-chlorophenyl) ketone → 1-(4-Chlorophenyl)-1-(2,2-difluorocyclopropyl)ethanol

HRID 561458
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HRID 561458 반응식
[CH3:1][Mg]Br.[Cl:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([CH:13]2[CH2:15][C:14]2([F:17])[F:16])=[O:12])=[CH:7][CH:6]=1>C(OCC)C>[Cl:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]([CH:13]2[CH2:15][C:14]2([F:16])[F:17])([OH:12])[CH3:1])=[CH:9][CH:10]=1
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참가 물질

4

반응물 2

HCID 248658712,2-Difluorocyclopropyl(4-chlorophenyl) ketoneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 583922561-(4-Chlorophenyl)-1-(2,2-difluorocyclopropyl)ethanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

5.7 ml (17.1 mmol) of a 3N solution of methylmagnesium bromide in diethyl ether were added to 2.47 g (11.4 mmol) of the compound from Example 124A in 40 ml of diethyl ether at RT, and the mixture was stirred at RT overnight. The reaction mixture was added to a saturated, ice-cold aqueous ammonium chloride solution, the phases were separated, the aqueous phase was extracted with dichloromethane, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate gradient) to result in 2.09 g (78% of theory) of a mixture of the diastereomers of the title compound.

후처리

  1. additionThe reaction mixture was added to a saturated, ice-cold aqueous ammonium chloride solution
  2. customthe phases were separated
  3. extractionthe aqueous phase was extracted with dichloromethane
  4. dry with materialthe combined organic phases were dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate gradient)

출처 및 근거

ORD 기록
ord-e45977603075426dacc7046eda30898d
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063234B2

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