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Water → 2-Bromo-2,6-dichloro-6-fluorocyclohexanol

HRID 399332
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HRID 399332 반응식
B(Br)(Br)[Br:2].[Cl:5][C:6]12O[CH:11]1[CH2:10][CH2:9][C:8]([Cl:14])([F:13])[CH2:7]2.[OH2:15]>ClCCl>[Br:2][C:6]1([Cl:5])[CH2:11][CH2:10][CH2:9][C:8]([Cl:14])([F:13])[CH:7]1[OH:15]
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참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 189709661,3-Dichloro-3-fluoro-7-oxabicyclo[4.1.0]heptane

생성물 1

HCID 189709682-Bromo-2,6-dichloro-6-fluorocyclohexanol

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

2.91 cm3 (2.91 mmol) of BBr3 in molar solution in dichloromethane were introduced at 4° C. under argon atmosphere into 0.98 (5.3 mmol) of epoxide 2e in solution in 6.5 cm3 dichloromethane. The reaction mixture was then allowed to return to room temperature and stirring was continued (1 h 30 min). 5 cm3 of distilled water were then added and the mixture was extracted with dichloromethane (4×10 cm3). The extract was dried over MgSO4, filtered and evaporated down. The crude product was purified by flash chromatography on silica (eluent ether/petroleum ether=5/95): 1.03 g of alcohol 1i were obtained (macrobore GC purity>97%); the yield of product 1i was 73%.

후처리

  1. customto return to room temperature
  2. custom(1 h 30 min)
  3. extractionthe mixture was extracted with dichloromethane (4×10 cm3)
  4. dry with materialThe extract was dried over MgSO4
  5. filtrationfiltered
  6. customevaporated down
  7. customThe crude product was purified by flash chromatography on silica (eluent ether/petroleum ether=5/95)

출처 및 근거

ORD 기록
ord-9f1f4514115346af92551ecb861db111
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05817890

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