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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423627Generated: October 30, 2026

4-Piperidinemethanol → {1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol

https://huagongshe.com/reaction/423627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidinemethanolHCID 420771—
Reactant3-(Propan-2-yl)-5-(trichloromethyl)-1,2,4-oxadiazoleHCID 50986551—
SolventMethanolHCID 887—
Product{1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanolHCID 5793007634.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 3-(1-methylethyl)-5-(trichloromethyl)-1,2,4-oxadiazole (prepared as in Example 158, Alternative synthesis, Step 3, 179 g, 0.78 mol) in MeOH (300 mL) was treated with 4-piperidinemethanol (108 g, 0.94 mol) and stirred and heated at 50° C. overnight. The solvent was removed and the residue was purified by flash chromatography on a silica gel column to give {1-[3-(1-methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol (60 g, 34%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101634B2
Source datasetuspto-grants-2012_01
ORD IDord-64109180c6cf4a6ebad82578caba18e2
Source noteuspto-grants-2012_01