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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274287Generated: October 26, 2026

Hydrochloric Acid → 4-Hydroxy-3,3-dimethyl-1-butanesulfonamide

https://huagongshe.com/reaction/274287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2,2-dimethyl-4-sulfamoylbutanoateHCID 10775463—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-Hydroxy-3,3-dimethyl-1-butanesulfonamideHCID 1074991777.2%

Reaction Steps

While a suspension of 0.35 g of lithium aluminum hydride in 30 ml of tetrahydrofuran was stirred with ice-cooling, a solution of 1.5 g of ethyl 4-aminosulfonyl-2,2-dimethylbutyrate in 8 ml of tetrahydrofuran was added dropwise. After completion of dropwise addition, the mixture was stirred at 0° C. for 30 minutes and, then, at room temperature for 30 minutes. To this reaction mixture was added aqueous tetrahydrofuran for decomposition of excess lithium aluminum hydride and the mixture was neutralized with 2N-hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and dried (MgSO4) and the solvent was distilled off. The residue was subjected to silica gel column chromatography and elution was carried out with hexane-ethyl acetate (1:1) to provide 0.94 g of the title compound. m.p.: 75°-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389633
Source datasetuspto-grants-1995_02
ORD IDord-cef947584fe1471b85f5dcdc74cab43f
Source noteuspto-grants-1995_02