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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625105Generated: October 31, 2026

1,2-Dichlorobenzene → Ethyl 5-phenyl-1,2,4-thiadiazole-3-carboxylate

https://huagongshe.com/reaction/625105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantBenzonitrileHCID 7505—
Reactantethyl 2-oxo-2H-1,3,4-oxathiazole-5-carboxylateHCID 12351252—
ProductEthyl 5-phenyl-1,2,4-thiadiazole-3-carboxylateHCID 123512543%

Reaction Steps

A mixture of ethyl 2-oxo-1,3,4-oxathiazole-5-carboxylate (U.S. Publication No. 2005/0096362) (1.5 g, 8.56 mmol) and benzonitrile (4.37 ml, 42.8 mmol) in 1,2-dichlorobenzene (15.42 ml, 137 mmol) was heated to 160° C. for 4 days. The reaction was then cooled down to RT and the solvent was evaporated by heated the reaction at 75° C. at maximum vacuum. The residue was purified on silica gel chromatography (100% CH2Cl2 to 3% EtOAc in CH2Cl2) to provide the title material (0.064 g, 3%). LC (Method B): 2.021 min. HRMS (ESI) calcd for C11H11N2O2S [M+H]+ m/z 235.0541, found 235. 1H NMR (CDCl3, 400 MHz) δ ppm: 8.01-8.09 (m, 1H), 7.49-7.59 (m, 2H), 4.56 (q, J=7.17 Hz, 1H), 1.50 (t, J=7.24 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303065B2
Source datasetuspto-grants-2016_04
ORD IDord-1632376b45314c1a8d7ca4fd2cc83cd1
Source noteuspto-grants-2016_04