HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-(5-Bromo-furan-2-yl)-[1,3,4]oxadiazole-2-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Bromofuran-2-carbohydrazide | HCID 468636 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(5-Bromo-furan-2-yl)-[1,3,4]oxadiazole-2-thiol | HCID 178527941 | — |
Reaction Steps
5-Bromo-furan-2-carboxylic acid hydrazide (20.5 g, 100 mmol) was added to a mixture of potassium hydroxide (6.2 g, 110 mmol) and methanol (125 ml). The mixture was stirred for 30 minutes at room temperature. Carbon disulfide (15.2 g, 200 mmol) was added. The mixture was stirred at reflux for 30 hours. Water (60 ml) was added and the excess of carbon disulfide and methanol was evaporated. The aqueous suspension was acidified by adding concentrated hydrochloric acid (14 ml). The product precipitated and was washed with water (20 ml), dried and evaporated. Yield 8.58 g (35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372832B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4f18b1e964144ee0bc28831be636126e |
| Source note | uspto-grants-2013_02 |