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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636662Generated: October 26, 2026

Benzene → (4-Methyl-1,2,3-thiadiazol-5-yl)(phenyl)methanone

https://huagongshe.com/reaction/636662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Methyl-1,2,3-thiadiazole-5-carboxylic acidHCID 1381992—
ReactantAluminum(III) ChlorideHCID 6451240—
Product(4-Methyl-1,2,3-thiadiazol-5-yl)(phenyl)methanoneHCID 1229899197%

Reaction Steps

To 2.0 g (15 mimol) of thionyl chloride was added 0.50 g (3.5 mmol) of 4-methyl-1,2,3-thiadiazole-5-carboxylic acid. After heating the mixture with stirring for 2 hours, the thionyl chloride was distilled off under reduced pressure, and the residue was added to a solution of 1.8 g (15 mmol) of aluminum chloride in 20 ml benzene and made to react with heating for 3 hours. After the reaction was completed, the reaction mixture was poured into ice water, the objective product was extracted with ethyl acetate, the organic layer was ashed with a saturated aqueous solution of sodium chloride and dried, the solvent was distilled off under educed pressure, and the residue was purified by silica gel column chromatography using 4:1 mixture of n-hexane and ethyl acetate. Thus, 0.69 g of the objective compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194444B1
Source datasetuspto-grants-2001_02
ORD IDord-2b7872b2bf45499d919201ef99717658
Source noteuspto-grants-2001_02