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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007332Generated: October 24, 2026

N-(4-chloro-2,5-dimethoxyphenyl)-3-fluoro-4-methoxybenzamide → N-(4-Chloro-2,5-dihydroxyphenyl)-3-fluoro-4-hydroxybenzamide

https://huagongshe.com/en/reaction/1007332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-chloro-2,5-dimethoxyphenyl)-3-fluoro-4-methoxybenzamideHCID 8409357—
SolventDichloromethaneHCID 6344—
ProductN-(4-Chloro-2,5-dihydroxyphenyl)-3-fluoro-4-hydroxybenzamideHCID 2190738191.3%

Reaction Steps

Boron trifluoride dimethyl sulfide complex (70 mL) was added into a mixture of N-(4-chloro-2,5-dimethoxyphenyl)-3-fluoro-4-methoxybenzamide (1.75 g, 5.15 mmol) and CH2Cl2 (35 mL). After stirring for 20 h, the solvent and the excess reagent were evaporated under a nitrogen stream in the hood. The residue was taken in a mixture of ice and HCl (1N) and extracted with EtOAc. The organic layer was washed with HCl (1N) and dried over MgSO4. Evaporation and purification by flash chromatography (CH2Cl2/hexanes/EtOAc 5/3/2, and AcOH 10 mL per 1 liter of the eluting solvent) gave a white solid (1.4 g, 91% yield, m.p. 254-256° C.); MS m/e 296 (M−H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794403B2
Source datasetuspto-grants-2004_09
ORD IDord-106ae1eea1f04c73a79ec916ab2bb3b0
Source noteuspto-grants-2004_09