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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580274Generated: October 25, 2026

Hydrochloric Acid → 2-Chloro-4-fluoro-5-aminophenyl methanesulfonate

https://huagongshe.com/reaction/580274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-4-fluoro-5-nitrophenyl methanesulfonateHCID 13798229—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product2-Chloro-4-fluoro-5-aminophenyl methanesulfonateHCID 1379823092.9%

Reaction Steps

A suspension of 2-chloro-4-fluoro-5-nitrophenyl methanesulfonate (27.0 g) and iron (33.5 g) in water (140 ml) was heated for reduction of the nitro group into amino group. When the temperature of the reaction mixture reached 80° C., 35% hydrochloric acid (3.2 g) was added thereto. Upon cooling to room temperature, the pH of the reaction mixture was adjusted to 9.0 with the addition of an aqueous sodium hydroxide solution. The reaction mixture was then extracted with toluene and tetrahydrofuran. The organic layer so separated was washed with water, dried over anhydrous sodium sulfate and then distilled under reduced pressure to remove the solvent, affording the titled compound (22.3 g) as a pale yellow oil which was then purified by silica gel chromatography to give colorless crystals with melting point 79°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04752326
Source datasetuspto-grants-1988_06
ORD IDord-fe01b259de49419b95da5a3a723218c8
Source noteuspto-grants-1988_06