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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354463Generated: October 27, 2026

Methyl 4-carbamothioylbenzoate → Methyl 4-[5-(4-trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoate

https://huagongshe.com/reaction/1354463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-carbamothioylbenzoateHCID 11401319—
ReactantN-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chlorideHCID 86593884—
SolventMethanolHCID 887—
ProductMethyl 4-[5-(4-trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoateHCID 2293453857%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride (1.55 g), methyl 4-thiocarbamoylbenzoate (0.976 g) and methanol (50 ml) was stirred at 50° C. for 2 hrs. After cooling, the crystals were collected by filtration to give methyl 4-[5-(4-trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoate (1.03 g, yield 57%) as a colorless crystalline powder. melting point: 218–219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223791B2
Source datasetuspto-grants-2007_05
ORD IDord-c6b70ee12ee84b749f89a8177368b91a
Source noteuspto-grants-2007_05