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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513005Generated: October 26, 2026

Hydrochloric Acid → 5-Chloro-2-(2,3-difluoro-6-methoxybenzyloxy)-4-nitrophenol

https://huagongshe.com/reaction/1513005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Difluoro-6-methoxybenzyl bromideHCID 4995861—
Reactant4-Chloro-5-nitrocatecholHCID 12873364—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Chloro-2-(2,3-difluoro-6-methoxybenzyloxy)-4-nitrophenolHCID 5930984997.5%

Reaction Steps

To a solution of 4-chloro-5-nitrocatechol (10.4 g) in N,N-dimethylformamide (55 mL) was added sodium hydride (55%, 5.04 g) under ice-cooling, and the mixture was stirred at the same temperature for 10 minutes. To the reaction mixture was added N,N-dimethylformamide (11 mL), followed by adding a solution of 2,3-difluoro-6-methoxy-benzyl bromide (14.3 g) in N,N-dimethylformamide (22 mL) under ice-cooling, and the mixture was stirred at the same temperature for 10 minutes, and then stirred at room temperature for 1.5 hours. The reaction mixture was diluted with water. The mixture was poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=7/3−1/1) to give the title compound (18.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217069B2
Source datasetuspto-grants-2012_07
ORD IDord-5232a465ce844a38a03d462ab33565c0
Source noteuspto-grants-2012_07