(Bis(2-methoxyethyl)amino)sulfur trifluoride → 4-Bromo-1-chloro-2-(1-fluoroethyl)benzene

HRID 1988536Notes

Reaction equation

HRID 1988536 reaction equation
COCCN(S(F)(F)[F:11])CCOC.[Br:14][C:15]1[CH:16]=[CH:17][C:18]([Cl:24])=[C:19]([CH:21](O)[CH3:22])[CH:20]=1>ClCCl.O>[Br:14][C:15]1[CH:16]=[CH:17][C:18]([Cl:24])=[C:19]([CH:21]([F:11])[CH3:22])[CH:20]=1

Participants

5

Conditions

Temperature
0 °C

Procedure

Bis(2-methoxyethyl)aminosulfur trifluoride (4.5 g, 20.34 mmol) was added to a stirred solution of 1-(5-bromo-2-chlorophenyl)ethanol (3.99 g, 16.95 mmol) in dichloromethane (50 mL) at 0° C. The resulting solution was stirred at 0° C. for 3 h. The reaction mixture was quenched with a 5% solution of aquous sodium bicarbonate (100 mL) and the resulting bubbling biphasic reaction mixture was vigorously stirred at 0° C. for 15 m. The reaction mixture was diluted with water (50 mL) and extracted with dichloromethane twice. The combined organic layers were washed with 1M hydrochloric acid, dried and concentrated by rotary evaporation. The product was purified by flash chromatography on silica gel (hexanes) to yield the title compound (2.65 g, 11.16 mmol, 65.8% yield) as a clear oil: 1H NMR (CDCl3): δ 7.65 (d, 1H), 7.37 (m, 1H), 7.20 (m, 1H), 5.88 (dq, 1H), 1.61 (dd, 3H).

Workup

  1. customThe reaction mixture was quenched with a 5% solution of aquous sodium bicarbonate (100 mL)
  2. customthe resulting bubbling
  3. custombiphasic reaction mixture
  4. stirringwas vigorously stirred at 0° C. for 15 m
  5. extractionextracted with dichloromethane twice
  6. washThe combined organic layers were washed with 1M hydrochloric acid
  7. customdried
  8. concentrationconcentrated by rotary evaporation
  9. customThe product was purified by flash chromatography on silica gel (hexanes)

Sources & evidence

ORD record
ord-52d913690c784d5b95cd7657c4e263d6
Source dataset
uspto-grants-2010_01
Patent number
US07642220B2

Reaction notes

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