Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710085Generated: October 30, 2026

p-Toluenesulfonic acid → 2-(1-Benzylpiperidin-4-yl)-5-bromobenzo[d]oxazole

https://huagongshe.com/reaction/710085

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-benzyl-N-(5-bromo-2-hydroxyphenyl)piperidine-4-carboxamideHCID 71114186—
SolventO-XyleneHCID 7237—
Product2-(1-Benzylpiperidin-4-yl)-5-bromobenzo[d]oxazoleHCID 7111418724.3%

Reaction Steps

Intermediate 22 (47.6 g, 0.122 mol) was dissolved in xylene (500 ml) and added p-Toluenesulphonic acid (46 g, 0.24 mol). This mixture was refluxed for 20 h under a dean-stark condenser. Xylene was removed and pH of the residue was adjusted to 9 using aq NaHCO3 solution. Work up (EtOAc/H2O) afforded the crude. Crude was purified by column on 60-120 mesh silicagel using a gradient mixture of EtOAc and Petether (10:90) as eluent to afford the titled compound (11 g) as brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181214B2
Source datasetuspto-grants-2015_11
ORD IDord-0675eb050bb04621ad7564d762611032
Source noteuspto-grants-2015_11