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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287717Generated: October 26, 2026

Hydrochloric Acid → 3-Nitro-5-sulphamyl-4-(m-trifluoromethylphenoxy)-benzoic acid

https://huagongshe.com/reaction/1287717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
Reactant4-Chloro-3-nitro-5-sulphamoylbenzoic acidHCID 89893—
SolventSodium BicarbonateHCID 516892—
Product3-Nitro-5-sulphamyl-4-(m-trifluoromethylphenoxy)-benzoic acidHCID 21312153—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 4-chloro-3-nitro-5-sulphamyl-benzoic acid (7 g), m-trifluoromethylphenol (20 g), and 1N sodium bicarbonate (100 ml) was stirred at 95° C for 6 hours. Then the reaction mixture was acidified by the addition of 4N hydrochloric acid and the excess of trifluoromethylphenol was removed by steam distillation. After cooling, the precipitated 3-nitro-5-sulphamyl-4-(m-trifluoromethylphenoxy)-benzoic acid was collected by suction and recrystallized several times from methanol-water. The melting point of the pure compound was 205°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985777
Source datasetuspto-grants-1976_10
ORD IDord-b9536b1eceea461d8d566f5898cecd27
Source noteuspto-grants-1976_10