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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385867Generated: November 1, 2026

Water → HCID 178420907, compound

https://huagongshe.com/reaction/1385867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantOxan-2-ylmethyl methanesulfonateHCID 288115—
ReactantHCID 178527894HCID 178527894—
SolventMethanolHCID 887—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 178420907HCID 178420907—

Reaction Steps

9.7 g (173 mmol) of potassium hydroxide and 17.5 g (173 mmol) of 3-mercapto-1,2,4-triazole were dissolved in 200 ml of methanol and heated under reflux for one hour. After the solvent had been distilled off under reduced pressure, the residue was dried by azeotropic distillation with toluene and then taken up in 300 ml of methanol. 33.6 g (173 mmol) of tetrahydropyran-2-ylmethyl methanesulfonate (step a) were then added and the mixture was stirred at room temperature for 24 hours. 200 ml of water and 200 ml of methyl tert-butyl ether were then added to the reaction mixture and the organic phase was separated off, washed with water and dried. The mixture was concentrated and the residue was chromatographed over silica gel, yielding 18.2 g (53% of theory) of a yellow oil. (1H-NMR (CDCl3; δ in ppm): 8.05 (s,1H); 4.15 (d,1H); 3.65 (m,1H); 3.50 (m,1H); 3.25-3.10 (m,2H); 1.85 (m,1H); 1.75-1.25 (m,6H))

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265352B1
Source datasetuspto-grants-2001_07
ORD IDord-9cd1dde2f24c4884b9be4c8e9c0d13bd
Source noteuspto-grants-2001_07