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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265608Generated: October 29, 2026

3,4-dihydro-2H-pyran → HCID 69688429, compound

https://huagongshe.com/reaction/1265608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 69688420HCID 69688420—
SolventEthyl AcetateHCID 8857—
ProductHCID 69688429HCID 69688429—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 3-(5-hydroxymethyl-[1,3,4]oxadiazol-2-yl)-benzoic acid methyl ester (9.8 g), dihydropyrane (7.7 mL) and p-toluenesulfonic acid hydrate (0.80 g) in AcOEt (100 mL) was stirred at 20° C. for 1 h. The solution was diluted with AcOEt, washed with 5% NaHCO3 solution and with brine, dried and evaporated. The residual oil was purified by chromatography on silica gel using AcOEt/hexane (1:2) as eluent to give 3-[5-(tetrahydro-pyran-2-yloxymethyl)-[1,3,4]thiadiazol-2-yl]-benzoic acid methyl ester (12.6 g) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544985B2
Source datasetuspto-grants-2003_04
ORD IDord-318a1ba44d5945eeb011927c210dedca
Source noteuspto-grants-2003_04