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4-Chlorophenol → 3,3-Bisfluoromethyl-1-(4-chlorophenoxy)-butan-2-one

HRID 2198764
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인쇄 미리보기

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HRID 2198764 반응식
[F:1][CH2:2][C:3]([CH2:9][F:10])([CH3:8])[C:4](=[O:7])[CH2:5]Br.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[F:1][CH2:2][C:3]([CH2:9][F:10])([CH3:8])[C:4](=[O:7])[CH2:5][O:18][C:15]1[CH:16]=[CH:17][C:12]([Cl:11])=[CH:13][CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 46844-ChlorophenolHCID 11430Potassium CarbonateHCID 130194343,3-Bisfluoromethyl-1-bromo-butan-2-one

생성물 1

HCID 130194353,3-Bisfluoromethyl-1-(4-chlorophenoxy)-butan-2-one수율 91.8%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
40 °C

실험 절차

171.2 g (0.79 mol) of 3,3-bisfluoromethyl-1-bromo-butan-2-one were added dropwise to a stirred mixture of 102 g (0.79 mol) of p-chlorophenol and 110 g (0.79 mol) of powdered potassium carbonate in 500 ml of acetone at 20° to 30° C. The mixture was subsequently stirred at 40° C. for 4 hours, the inorganic salt was filtered off and the filtrate was concentrated. The residue was distilled under a high vacuum. 190.5 g (90% of theory) of 3,3-bisfluoromethyl-1-(4-chlorophenoxy)-butan-2-one of boiling point 113°-117° C./0.1 mm Hg were obtained. ##STR74##

후처리

  1. filtrationthe inorganic salt was filtered off
  2. concentrationthe filtrate was concentrated
  3. distillationThe residue was distilled under a high vacuum

출처 및 근거

ORD 기록
ord-1dc16f445edd4ea9ba6a67ffc5499887
출처 데이터셋
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04359470

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