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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245271Generated: October 29, 2026

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

https://huagongshe.com/reaction/245271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
Reactant1-(5-Bromo-2-chlorophenyl)ethanolHCID 58762644—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-chloro-2-(1-fluoroethyl)benzeneHCID 5912694765.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658791B2
Source datasetuspto-grants-2014_02
ORD IDord-a272d6206e164cd8bf2782c465e6bf64
Source noteuspto-grants-2014_02