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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant2,8-Dimethyl-1-oxa-8-azaspiro[4.5]decan-3-oneHCID 10176401—
SolventEthanolHCID 702—
ProductAmmoniaHCID 222—
Product3-Hydroxy-2,8-dimethyl-1-oxa-8-azaspiro[4.5]decaneHCID 10397520197.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412096
Source datasetuspto-grants-1995_05
ORD IDord-0370b22b60c349228458cfb51242cdd1
Source noteuspto-grants-1995_05