Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265609Generated: November 1, 2026

3,4-dihydro-2H-pyran → HCID 69689153, compound

https://huagongshe.com/reaction/1265609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 69688087HCID 69688087—
SolventEthyl AcetateHCID 8857—
ProductHCID 69689153HCID 69689153—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 3-[5-(2-hydroxy-ethyl)-[1,3,4]oxadiazol-2-yl]-benzoic acid methyl ester (7.45 g), dihydropyrane (4.1 mL) and p-toluenesulfonic acid hydrate (0.57 g) in AcOEt (80 mL) was stirred at 20° C. for 2 h. The solution was diluted with AcOEt, washed with 5% NaHCO3 solution and with brine, dried and evaporated in vacuum. The residual oil was purified by chromatography on silica gel using AcOEt/hexane (1:2) as eluent to give 3-{5-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-[1,3,4]thiadiazol-2-yl}-benzoic acid methyl ester (8.2 g) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544985B2
Source datasetuspto-grants-2003_04
ORD IDord-e8ecdd3f21754020b4e0217898a7a330
Source noteuspto-grants-2003_04