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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66945Generated: October 28, 2026

2,4-Dichlorobenzoyl chloride → 5-(2,4-Dichlorobenzamido)-3-Trichloromethyl-1,2,4-Thiadiazole

https://huagongshe.com/reaction/66945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzoyl chlorideHCID 66645—
Reactant3-(Trichloromethyl)-1,2,4-thiadiazol-5-amineHCID 602848—
SolventO-XyleneHCID 7237—
Product5-(2,4-Dichlorobenzamido)-3-Trichloromethyl-1,2,4-ThiadiazoleHCID 1304152469.5%

Reaction Steps

A solution of 10.9 g (0.05 mole) 5-amino-3-trichloromethyl-1,2,4-thiadiazole and 20.9 g (0.10 mole) 2,4-dichlorobenzoyl chloride was refluxed in 200 ml xylene for 20 hours. The reaction mixture was concentrated in vacuo and the resulting residue extracted with benzene. Addition of hexane resulted in precipitation of 13.6 g (69% yield) pure product; m.p. 136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343945
Source datasetuspto-grants-1982_08
ORD IDord-5ed551a71a4646b6861ec463374c3df0
Source noteuspto-grants-1982_08