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

HRID 399332
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 399332
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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Komponenten

5

Edukt 3

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

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

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%.

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-9f1f4514115346af92551ecb861db111
Quelldatensatz
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05817890

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