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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074221Generated: October 26, 2026

Phenol → Phenol

https://huagongshe.com/reaction/1074221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
Reactant1,1,2-TrichloroethaneHCID 6574—
ReactantN-Fluoro-6-chloropyridinium-2-sulfonateHCID 14897827—
ProductPhenolHCID 996—
Product2-FluorophenolHCID 9707—

Reaction Steps

A 25 ml egg-plant type flask was flushed with argon, and 42.4 mg (0.45 mmol) of phenol, 2 ml of dry 1,1,2-trichloroethane and 95.3 mg (0.45 mmol) of N-fluoro-2-chloropyridinium-6-sulfonate were charged. The flask was immersed in an oil bath of 100° C. and heated for 49 hours. After completion of the reaction, the reaction solution was washed with water to remove 2-chloropyridine-6-sulfonic acid. The organic layer was quantitatively analyzed by gas chromatography. o-Fluorophenol was obtained at a conversion yield of 58%, and phenol was recovered at a recovery rate of 5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04973697
Source datasetuspto-grants-1990_11
ORD IDord-f5911b1e5b8140889c928cace3bd7b3a
Source noteuspto-grants-1990_11