Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984076Generated: October 28, 2026

4-Piperidinecarboxylic acid → 2-(Piperidin-4-yl)-1,3-benzoxazole

https://huagongshe.com/reaction/984076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acidHCID 3773—
Reactant2-AminophenolHCID 5801—
ReactantPotassium HydroxideHCID 14797—
SolventWaterHCID 962—
Product2-(Piperidin-4-yl)-1,3-benzoxazoleHCID 77046184.3%

Reaction Conditions

Temperature180 °C

Reaction Steps

2-Aminophenol (200 mg) and 4-piperidinecarboxylic acid (236 mg) were mixed with polyphosphoric acid (1 g) and stirred with heating at 180° C. for 2 hours. After cooling to room temperature, the reaction was stopped by adding water. The filtrate was adjusted to pH 12 with 50% potassium hydroxide aqueous solution and then extracted with methylene chloride. The organic layer was washed with saturated brine and dried with magnesium sulfate, and then the solvent was evaporated under a reduced pressure to obtain the title compound 2-(4-piperidyl)benzoxazole (311.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867226B2
Source datasetuspto-grants-2005_03
ORD IDord-5a673342a17d4a358448b3a8235e5104
Source noteuspto-grants-2005_03