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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722921Generated: October 30, 2026

Water → 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)nitrobenzene

https://huagongshe.com/reaction/1722921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenol, 2-chloro-4-fluoro-5-nitro-HCID 158655—
Reactant2-(Bromomethyl)-1,1-difluorocyclopropaneHCID 2761402—
SolventDimethylformamideHCID 6228—
Product4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)nitrobenzeneHCID 14129431—

Reaction Steps

3.6 g 2-Chloro-4-fluoro-5-nitrophenol was dissolved in dimethylformamide and treated with potassium carbonate. The mixture was stirred at room temperature for one hour and then 3.3 g 2,2-difluorocyclopropylmethyl bromide added. It was the heated at 80° C. for 2 hours and added to water. The mixture was extracted with methylene chloride and the organic phase washed with saturated brine, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel using a mixture of 3 parts hexane and 1 part ethyl acetate. There was obtained 5 g (=93% of theory) of yellow crystals whose nmr spectrum is as follows: δ=1.1-2.4 ppm (m) 3H, δ=4.15 ppm (d 7 Hz,tr 1.5 Hz) 2H, δ=7.35 ppm (d 10 Hz) 1H, δ=7.5 ppm (d 7 Hz) 1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859230
Source datasetuspto-grants-1989_08
ORD IDord-0f2e047be0434378acb8cf00e7bd41a0
Source noteuspto-grants-1989_08