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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911492Generated: October 25, 2026

Hydrochloric Acid → 5-Chloro-2-(difluoromethoxy)phenol

https://huagongshe.com/reaction/1911492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-ChlorocatecholHCID 16496—
ReactantSodium chlorodifluoroacetateHCID 2734985—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-2-(difluoromethoxy)phenolHCID 8676217719.4%

Reaction Conditions

Temperature125 °C

Reaction Steps

723 mg (5.0 mmol) of sodium chlorodifluoroacetate, 220 mg (5.5 mmol) of sodium hydroxide and 838 mg (5.5 mmol) of 4-chlorocatechol were successively added to a mixture of 7.0 mL of N,N-dimethylformamide and 0.1 mL of water under argon atmosphere with stirring. The mixture was slowly heated to 125° C. and allowed to react at this temperature for 1.0 h. The reaction was stopped and cooled to room temperature. To the reaction solution was added 10 mL of 1.0 mol/L hydrochloric acid until the solution turned acid, and then 50 mL of water and 20 mL of ethyl acetate were added. The organic layer was isolated, and the water layer was extracted with 20 mL×2 of ethyl acetate. The organic layers were combined, successively washed with 50 mL of water and 50 mL of saturated saline, dried over anh. MgSO4, filtered and concentrated. The residue was purified by preparative silica gel thin layer chromatography (mobile phase: petroleum ether: ethyl acetate=4:1) to obtain 189 mg of a light yellow oil. Yield 19.4%. MS([M-H]−): 193.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604065B2
Source datasetuspto-grants-2013_12
ORD IDord-ad20af7b85f1472991778f84fdfb0b66
Source noteuspto-grants-2013_12