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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992475Generated: October 26, 2026

Hydrochloric Acid → 4-Sulfamoylbenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/992475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantSulfanilamideHCID 5333—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Sulfamoylbenzene-1-sulfonyl chlorideHCID 10956159—

Reaction Steps

To a mixed solution of 80 ml water and 50 ml of concentrated hydrochloric acid was added 25.0 g (145 mmol) of 4-aminobenzenesulfonamide followed by stirring. An aqueous solution (20 ml) of 10.5 g (152 mmol) of sodium nitrite was added dropwise thereinto at −13° C. to −10° C. during 15 min. After 10 min, the reaction solution was added to a mixed solution saturated with sulfur dioxide (prepared by saturating sulfur dioxide in a mixed solution of 150 ml of acetic acid and 12.5 ml of concentrated hydrochloric acid followed by adding 3. 7 g of cuprous chloride) at −30° C. under stirring. After 1 hr, 500 ml of ice water was added to the reaction solution, and the resulting precipitates were collected by filtration. The precipitates were dissolved in a mixed solution of 450 ml of toluene and 150 ml of ethyl acetate. After the resulting insoluble matters were filtered off, the filtrate was extracted with ethyl acetate. The organic layer was washed with a saturated sodium bicarbonate solution and brine successively, and dried over magnesium sulfate. The solvent was evaporated, 100 ml of toluene was added to the resulting residue and the crystals were collected by filtration to give20.9 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469043B1
Source datasetuspto-grants-2002_10
ORD IDord-f69e2fcb429a4c5e91abd61e19461b60
Source noteuspto-grants-2002_10