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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782594Generated: October 26, 2026

Sodium hydride → 1-Bromo-4-chloro-3-(2,2-difluoroethoxy)-2-fluorobenzene

https://huagongshe.com/reaction/1782594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,2-Difluoroethyl methanesulfonateHCID 56776492—
Reactant3-Bromo-6-chloro-2-fluorophenolHCID 66601002—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Bromo-4-chloro-3-(2,2-difluoroethoxy)-2-fluorobenzeneHCID 8661384045.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-bromo-6-chloro-2-fluorophenol (15.4 g, 0.068 mol) in DMF (25 mL) was slowly added to a suspension of sodium hydride (60% dispersion in mineral oil) (4.0 g, 0.10 mol) in DMF (100 mL) and the mixture was stirred 1 hour. A solution of methanesulfonic acid 2,2 difluoroethyl ester (17.5 g, 0.109 mol) in DMF (10 mL) was slowly added. The resulting solution was heated to 70° C. for 18 hours. The solution was diluted with water (200 mL) and extracted with ethyl ether. The combined organic phases were dried (sodium sulfate) and concentrated. The residual oil was purified by chromatography (in hexanes) to give 1-bromo-4-chloro-3-(2,2-difluoroethoxy)-2-fluorobenzene (9.0 g, 0.031 mol): 1H NMR (CDCl3): δ 7.3 (m, 1H), 7.10 (dd, 1H), 6.15 (dt, 1H), 4.35 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498468B2
Source datasetuspto-grants-2009_03
ORD IDord-c5668ed9c68646b79a8599eb7a65ab66
Source noteuspto-grants-2009_03