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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252052Generated: November 2, 2026

Hydrochloric Acid → Benzenesulfonamide, 4-(hydroxymethyl)-N-methyl-

https://huagongshe.com/reaction/2252052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-(Methylsulfamoyl)benzoic acidHCID 506056—
SolventTetrahydrofuranHCID 8028—
ProductBenzenesulfonamide, 4-(hydroxymethyl)-N-methyl-HCID 1798176875%

Reaction Conditions

Temperature80 °C

Reaction Steps

Add methyl amine (4.5 mL, 2 M in dichloromethane) to a mixture of 4-chlorosulfonyl benzoic acid (0.5 g) and dichloromethane (20 mL). Stir at room temperature overnight. Quench by pouring the reaction mixture into a mixture of saturated aqueous ammonium chloride and ethyl acetate. Separate the layers, wash the organic phase with water, dry the remaining organic phase over sodium sulfate and then concentrate under reduced pressure to provide (0.40 g, 82%) of an oil. Add borane-tetrahydrofuran complex (7.44 mL, 1 M) to a mixture of 4-methylsulfamoyl-benzoic acid (0.4 g) and tetrahydrofuran (10 mL) at 0° C. Heat at 80° C. for 3 hours. Cool at room temperature and add 1 N aqueous hydrochloric acid (20 mL) and extract with ethyl acetate. Wash with saturated aqueous sodium bicarbonate and dry the remaining organic phase over sodium sulfate and concentrate under reduced pressure to provide (0.28 g, 75%) of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320995B2
Source datasetuspto-grants-2008_01
ORD IDord-f707af3d727648f9a6a8a483e0334c30
Source noteuspto-grants-2008_01