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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486050Generated: October 30, 2026

Ozone → HCID 19097394, compound

https://huagongshe.com/reaction/486050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19097423HCID 19097423—
SolventEthanolHCID 702—
ProductHCID 19097394HCID 1909739495%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2,3,4-trimethyl-3-(3-methyl-2-buten-1-yl)-1-(phenylmethyl)piperidine hydrochloride (24.7 g, 76.7 mmol) was dissolved in ethanol (500 mL) and cooled to -78° C. ozone was bubbled into the reaction mixture until the solution turned blue and the mixture was purged with oxygen, then nitrogen until the solution turned colorless. Sodium borohydride (14.5 g, 383 mmol) was added to the reaction mixture while maintaining the temperature at -78° C. and the solution was stirred at -78° C. for 1 hour. The mixture was slowly warmed to room temperature over a period of 2 hours, 6 H HCl was added to acidify the solution and the solvent was removed in vacuo. The white residue was taken up in water, washed with ether (3×100 mL), basified with aqueous NAOH and extracted with methylene chloride (3×200 mL) The organic layer was dried over Na2SO4 and the solvent was removed in vacuo. The residue was taken up in ether (500 mL), dried over anhydrous MgSO4 and the solvent was removed in vacuo to afford 19.1 g (95%) of 2,3,4-trimethyl-1-(phenylmethyl)-3-piperidineethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290789
Source datasetuspto-grants-1994_03
ORD IDord-ae5a1b64b0bc42048d1e383c65a42379
Source noteuspto-grants-1994_03