HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(4-Chloro-2-methylphenyl)-1,2,3-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | ethyl N-[(E)-1-(4-chloro-2-methylphenyl)ethylideneamino]carbamate | HCID 145779288 | — |
| Product | 4-(4-Chloro-2-methylphenyl)-1,2,3-thiadiazole | HCID 21866160 | — |
Reaction Steps
Ethyl (2E)-2-[1-(4-chloro-2-methylphenyl)ethylidene]hydrazine carboxylate (0.63 g, 2.45 mmol) was stirred with thionyl chloride (1 mL, 13.70 mmol) at 60° C. for 1 h. The mixture was cooled to room temperature and concentrated in vacuo. 4-(4-Chloro-2-methylphenyl)-1,2,3-thiadiazole was obtained as a red solid. MS m/z=211.5; 1H NMR (CDCl3, 400 MHz) δ 2.45 (s, 3H), 7.31 (dd, J=2.2, 8.2 Hz, 1H), 7.36 (d, J=1.8 Hz, 1H), 7.60 (d, J=8.2 Hz, 1H), 8.51 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07144899B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-5985d49596974f968ae550e062733b47 |
| Source note | uspto-grants-2006_12 |