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

HRID 506447
Notes
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Reaction equation

HRID 506447 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
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 2734690(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 587626441-(5-Bromo-2-chlorophenyl)ethanol

Product 1

HCID 591269474-Bromo-1-chloro-2-(1-fluoroethyl)benzeneYield 65.8%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6344DichloromethaneSolvent

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 aqueous sodium bicarbonate (100 mL) and the resulting bubbling biphasic reaction mixture was vigorously stirred at 0° C. for 15 min. 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 aqueous sodium bicarbonate (100 mL)
  2. customthe resulting bubbling
  3. custombiphasic reaction mixture
  4. stirringwas vigorously stirred at 0° C. for 15 min
  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-f3f14d11f69846369fc778c8c3249455
Source dataset
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07786044B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes