HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2-(1-Benzylpiperidin-4-yl)-5-bromobenzo[d]oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-benzyl-N-(5-bromo-2-hydroxyphenyl)piperidine-4-carboxamide | HCID 71114186 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(1-Benzylpiperidin-4-yl)-5-bromobenzo[d]oxazole | HCID 71114187 | 24.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181214B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-0675eb050bb04621ad7564d762611032 |
| Source note | uspto-grants-2015_11 |