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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225473Generated: October 26, 2026

1,4-Dioxane hydrochloride → 2-(Piperidin-4-YL)propane-1,3-diol hydrochloride

https://huagongshe.com/reaction/225473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantTert-butyl 4-(1,3-dihydroxypropan-2-yl)piperidine-1-carboxylateHCID 59605609—
SolventMethanolHCID 887—
Product2-(Piperidin-4-YL)propane-1,3-diol hydrochlorideHCID 67197231—

Reaction Steps

A mixture of 1-tert-butoxycarbonylpiperidine-4-ol, triethylamine, benzenesulfonyl chloride and methylene chloride was stirred for two days at room temperature to give 1-tert-butoxycarbonylpiperidine-4-ylbenzenesulfonate. A mixture of the obtained 1-tert-butoxycarbonylpiperidine-4-ylbenzenesulfonate, diethyl malonate, 20% sodium ethoxide-EtOH solution and EtOH was stirred for 22 hours heated to reflux to give diethyl[1-(tert-butoxycarbonyl)piperidine-4-yl]malonate. A mixture of the obtained diethyl[1-(tert-butoxycarbonyl)piperidine-4-yl]malonate, lithium borohydride, toluene and THF was stirred for 18 hours at 60° C. to give 2-(1-tert-butoxycarbonylpiperidine-4-yl)propane-1,3-diol. A mixture of the obtained 2-(1-tert-butoxycarbonylpiperidine-4-yl)propane-1,3-diol, 4M HCl-dioxane solution and MeOH was stirred for one hour at room temperature to give 2-piperidine-4-ylpropane-1,3-diol hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557112B2
Source datasetuspto-grants-2009_07
ORD IDord-5a24eae633374f0a94ef399cf9c6e8b2
Source noteuspto-grants-2009_07