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Propargyl bromide → 1-(Prop-2-ynyloxy)-2-(trifluoromethoxy)benzene

HRID 536450
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HRID 536450 반응식
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10].C(=O)([O-])[O-].[K+].[K+].[CH2:19](Br)[C:20]#[CH:21]>C(#N)C.O>[CH2:21]([O:10][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[O:3][C:2]([F:11])([F:12])[F:1])[C:20]#[CH:19]
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참가 물질

6

반응물 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 27772992-(Trifluoromethoxy)phenol

생성물 1

HCID 233934371-(Prop-2-ynyloxy)-2-(trifluoromethoxy)benzene수율 107.6%

시약·촉매·용매 2

HCID 962Water용매HCID 6342Acetonitrile용매

실험 절차

To a solution of 2-trifluoromethoxyphenol (10.0 g, 56.1 mmol) in acetonitrile (120 mL) was added potassium carbonate (9.31 g, 67.4 mmol) and propargyl bromide (80% in toluene, 10.0 g, 7.70 mL, 67.4 mmol). The reaction mixture was stirred at ambient temperature for seven days, then diluted with water (150 mL) and extracted with diethyl ether (300 mL). The organic layer was separated and concentrated to obtain the title compound (13.05 g) which was used without further purification in the next step.

후처리

  1. extractionextracted with diethyl ether (300 mL)
  2. customThe organic layer was separated
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e628bdc37ccd441c99c7eee47e218df7
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859584B2

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