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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250199Generated: November 1, 2026

Thiophenol → 4-Methyl-5-[(phenylthio)methyl]-1,2,3-thiadiazole

https://huagongshe.com/reaction/1250199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
ReactantThionyl ChlorideHCID 24386—
Reactant(4-Methyl-1,2,3-thiadiazol-5-yl)methanolHCID 18411623—
SolventAcetoneHCID 180—
Product4-Methyl-5-[(phenylthio)methyl]-1,2,3-thiadiazoleHCID 1590664085%

Reaction Steps

At an ice-cooled temperature, 3 ml of thionyl chloride was added to 0.50 g (3.8 mmol) of 4-methyl-1,2,3-thiadiazol-5-ylmethanol and stirred for 4 hours. Then, the reaction mixture was concentrated under reduced pressure, and 1.30 g (11.5 mmol) of potassium carbonate, 0.38 g (3.4 mmol) of thiophenol and 10 ml of acetone were added to the concentrate and reacted for 7 hours with heating under reflux. After the reaction was completed, the reaction mixture was cooled to room temperature, the precipitated matter was filtered off, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography using 5:1 mixture of n-hexane and ethyl acetate. Thus, 0.64 g of the objective compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337341B1
Source datasetuspto-grants-2002_01
ORD IDord-7b27486e4e0c4ef7bdc092a413e8d95d
Source noteuspto-grants-2002_01