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Boron tribromide → 1-(2-Hydroxy-5-(trifluoromethyl)phenyl)ethan-1-one

HRID 1402051
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HRID 1402051 반응식
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([F:12])([F:11])[F:10])=[CH:5][C:4]=1[C:13](=[O:15])[CH3:14].B(Br)(Br)Br>ClCCl.[I-].C([N+](CCCC)(CCCC)CCCC)CCC>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([F:10])([F:11])[F:12])=[CH:5][C:4]=1[C:13](=[O:15])[CH3:14]
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참가 물질

5

반응물 2

HCID 25134Boron tribromideHCID 99426011-(2-Methoxy-5-trifluoromethylphenyl)ethanone

생성물 1

HCID 117695991-(2-Hydroxy-5-(trifluoromethyl)phenyl)ethan-1-one수율 35.2%

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide촉매HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 1-[2-methoxy-5-(trifluoromethyl)phenyl]ethanone (35 g, 0.160 mol) in dry dichloromethane (400 mL) at 0° C. was added solid tetrabutylammonium iodide (2.96 g, 0.008 mol) followed by boron tribromide (33.96 mL, 0.353 mol) dropwise. After addition, the reaction mixture was stirred at room temperature for 90 minutes. The reaction mixture was cooled to 0° C. and quenched with ice. The mixture was extracted with diethyl ether (1000 mL). The organic layer was washed with water (2000 mL) and then saturated aqueous sodium chloride (1000 mL). After concentration of the organic layer at room temperature in vacuo, the crude product was purified by column chromatography (100-200 silica gel, 2% v/v diethyl ether in hexane) to give 11.5 g (35%) of the title compound as a colourless oil.

후처리

  1. additionAfter addition
  2. temperatureThe reaction mixture was cooled to 0° C.
  3. customquenched with ice
  4. extractionThe mixture was extracted with diethyl ether (1000 mL)
  5. washThe organic layer was washed with water (2000 mL)
  6. customAfter concentration of the organic layer at room temperature in vacuo, the crude product was purified by column chromatography (100-200 silica gel, 2% v/v diethyl ether in hexane)

출처 및 근거

ORD 기록
ord-7ef33f19a0b34095b003f9f38060a4d2
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08907101B2

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