HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274294Generated: October 26, 2026
Hydrochloric Acid → 5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide
https://huagongshe.com/reaction/274294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 5-aminosulfonyl-2,2-dimethylvalerate | HCID 10585962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide | HCID 10726520 | 58% |
Reaction Steps
A solution of 7.1 g of the ethyl 5-aminosulfonyl-2,2-dimethylvalerate obtained in Reference Example 26 in 20 ml of tetrahydrofuran was added dropwise to a suspension of 1.71 g of lithium aluminum hydride in 100 ml of tetrahydrofuran with ice-cooling and stirring. After completion of dropwise addition, the mixture was stirred at 0° C. for 40 minutes and after addition of aqueous tetrahydrofuran for decomposition of excess lithium aluminum hydride, 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 (100 g) column chromatography and elution was carried out with hexane-ethyl acetate (4:1) to provide 3.39 g of the title compound as oil.
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-ccac5104cfb04a02aa15ca8504d606db |
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| Source note | uspto-grants-1995_02 |
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