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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2447Generated: October 23, 2026

Hydrochloric Acid → 4-Hydroxymethyl-N-(2-methoxyphenyl)benzenesulfonamide

https://huagongshe.com/en/reaction/2447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant4-((2-Methoxyphenyl)sulfamoyl)benzoic acidHCID 2333505—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Hydroxymethyl-N-(2-methoxyphenyl)benzenesulfonamideHCID 1968990869.6%

Reaction Steps

In an atmosphere of argon and with cooling in an ice bath, 4-[(2-methoxyanilino)sulfonyl]benzoic acid (150 mg, 0.488 mmol) was dissolved in THF (5 ml), to which were subsequently added dropwise triethylamine (0.14 ml, 1.0 mmol) and ethyl chloroformate (50 μl, 0.509 mmol). After 30 minutes of stirring at the same temperature, the thus formed precipitate was removed by filtration, and the resulting filtrate was concentrated. The thus obtained residue was dissolved in 5 ml of THF, and, with cooling in an ice bath, sodium borohydride (46.5 mg, 1.22 mmol) and water (1 ml) were added to the resulting solution. After 40 minutes of stirring at the same temperature, the reaction mixture was adjusted to pH 4 to 5 with 2N hydrochloric acid and extracted with ether. The organic layer was washed with saturated brine and dried on anhydrous magnesium sulfate. After removing the solvent by evaporation, the resulting colorless oily material was purified by silica gel column chromatography (ether) to obtain 99.6 mg (69.6%) of the title compound in the form of colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728835
Source datasetuspto-grants-1998_03
ORD IDord-5fabbe4482ff451aa260f688512ff2dd
Source noteuspto-grants-1998_03