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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 2,2-dimethyl-4-sulfamoylbutanoate | HCID 10775463 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-3,3-dimethyl-1-butanesulfonamide | HCID 10749917 | 77.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389633 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-cef947584fe1471b85f5dcdc74cab43f |
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| Source note | uspto-grants-1995_02 |
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