HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Hexyl-5-(6-acetoxynaphthalene-2-yl)-1,3,4-thiadiazole | HCID 19907942 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole | HCID 136077200 | 74.3% |
Reaction Steps
1.50 g (22.7 mM) of potassium hydroxide was dissolved in 72 ml of ethanol at 60°-65° C. To the solution, 2.90 g (8.18 mM) of 2-hexyl-5-(6-acetoxynaphthalene-2-yl)-1,3,4-thiadiazole was added, followed by stirring for 20 minutes at 60°-65° C. The reaction mixture was poured into 200 ml of iced water and 3 ml of concentrated hydrochloric acid was added thereto to precipitate a crystal. The crystal was recovered by filtration and washed with water to obtain 1.90 g of 2-hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole (Yield: 71.9 %). ##STR138##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05091109 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-024ae5efd6834466b85091b87e28a033 |
| Source note | uspto-grants-1992_02 |