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Phosphorus tribromide → 5-Bromo-2-(bromomethyl)-1,3-difluorobenzene

HRID 576194
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HRID 576194 반응식
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH2:9]O)=[C:4]([F:11])[CH:3]=1.[Br:12]P(Br)Br>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH2:9][Br:12])=[C:4]([F:11])[CH:3]=1
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 27733034-Bromo-2,6-difluorobenzyl alcohol

생성물 1

HCID 27733055-Bromo-2-(bromomethyl)-1,3-difluorobenzene수율 61.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (4-bromo-2,6-difluorophenyl)methanol (2 g, 8.97 mmol) in DCM (80 mL) was added tribromophosphine (2.91 g, 10.76 mmol) at 0° C. The resulting mixture was stirred at rt. After LCMS analysis showed the starting material had disappeared, the mixture was washed with aq NaHCO3 (40 mL) and brine (30 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The crude material was purified by silica column chromatography (PE/EA=5/1) to yield a colorless oil of 5-bromo-2-(bromomethyl)-1,3-difluorobenzene (1.6 g, 5.48 mmol, 61.2% yield): 1H NMR (400 MHz, CD3OD) δ 7.12 (d, J=6.8 Hz, 2H), 4.47 (s, 2H).

후처리

  1. washthe mixture was washed with aq NaHCO3 (40 mL) and brine (30 mL)
  2. dry with materialThe organic layer was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude material was purified by silica column chromatography (PE/EA=5/1)

출처 및 근거

ORD 기록
ord-a013fe7219fa44e8b8bf167ec3cc5774
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09035063B2

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