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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992694Generated: November 2, 2026

Sodium Hydroxide → 2-Methyl-5-benzoylthiomethyl-1,3,4-thiadiazole

https://huagongshe.com/reaction/992694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-(Chloromethyl)-5-methyl-1,3,4-thiadiazoleHCID 15582007—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178526132HCID 178526132—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Methyl-5-benzoylthiomethyl-1,3,4-thiadiazoleHCID 18411604—

Reaction Steps

Under nitrogen atomosphere, thiobenzoic acid (2.52 ml) was added dropwise to a solution of potassium tert-butoxide (2.30 g) in DMF (15 ml) under ice cooling. After stirring for 10 minutes, 2-chloromethyl-5-methyl-1,3,4-thiadiazole in DMF (15 ml) was added to the mixture. The whole mixture was and stirred for 45 minutes. The mixture was poured into a mixture of water and ethyl acetate, and the pH was adjusted to 8.5 with 30% aqueous sodium hydroxide. Organic layer was separated, was washed with water and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was purified on silica gel (eluent: n-hexane-ethyllactate) to afford 2-methyl-5-benzoylthiomethyl-1,3,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468995B1
Source datasetuspto-grants-2002_10
ORD IDord-3151123e922d40178cc0b9f9a7e29952
Source noteuspto-grants-2002_10