HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichlorobenzene → Ethyl 5-phenyl-1,2,4-thiadiazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | ethyl 2-oxo-2H-1,3,4-oxathiazole-5-carboxylate | HCID 12351252 | — |
| Product | Ethyl 5-phenyl-1,2,4-thiadiazole-3-carboxylate | HCID 12351254 | 3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303065B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-1632376b45314c1a8d7ca4fd2cc83cd1 |
| Source note | uspto-grants-2016_04 |