HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36005Generated: October 24, 2026
Hydrochloric Acid → 3-Hydroxy-2,8-dimethyl-1-oxa-8-azaspiro[4.5]decane
https://huagongshe.com/en/reaction/36005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,8-Dimethyl-1-oxa-8-azaspiro[4.5]decan-3-one | HCID 10176401 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ammonia | HCID 222 | — |
| Product | 3-Hydroxy-2,8-dimethyl-1-oxa-8-azaspiro[4.5]decane | HCID 10397520 | 197.8% |
Reaction Steps
To a solution of 2,8-dimethyl-1-oxa-8-azaspiro[4,5]-decan-3-one (200 mg) in 7 ml ethanol, was added 25 mg sodium borohydride at room temperature, and the mixture was stirred at room temperature for two hours. The reaction mixture was cooled in an ice-water bath, acidified by addition of 6N-HCl (to about pH 4), and stirred for about 20 minutes with the ice-water bath removed. Ethanol was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography by using, as eluent, a mixed solvent of chloroform/methanol/conc. ammonia (5:1:0.1 by volume), giving 200 mg of 3-hydroxy-2,8-dimethyl-1-oxa-8-azaspiro[4,5]decane as oil. It was dissolved in ether, and ethanolic hydrogen chloride was added to this solution, thus giving its hydrochloride as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05412096 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-0370b22b60c349228458cfb51242cdd1 |
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| Source note | uspto-grants-1995_05 |
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