HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Ethyl 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Ethyl cyanoformate | HCID 69336 | — |
| Reactant | 5-(4-Methoxyphenyl)-1,3,4-oxathiazol-2-one | HCID 819456 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | Ethyl 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylate | HCID 12601460 | 77% |
Reaction Steps
Ethyl cyanoformate (16.9 g, 0.171 mol) is added to a stirred solution of 5-(4-methoxyphenyl)-[1,3,4]oxathiazolin-2-one (11.9 g, 0.057 mol) in p-xylene (100 ml). The mixture is heated to 115°-132° C. for 10 hours, during which time carbon dioxide is liberated. The solvent is evaporated in vacuo and the residue is triturated with di-isopropyl ether. The crystalline solid is filtered off, washed with a small amount of diisopropyl ether and dried, to give ethyl 3-(4-methoxyphenyl)-[1,2,4]thiadiazole-5-carboxylate (11.6 g, 77%) as beige crystals, m.p. 61°-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05583092 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-839da68b54ff4eecbda9b2d3fd9e2f68 |
| Source note | uspto-grants-1996_12 |