HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 6-Phenylimidazo(2,1-b)(1,3,4)thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 1,3,4-Thiadiazol-2-amine | HCID 19909 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Phenylimidazo(2,1-b)(1,3,4)thiadiazole | HCID 853547 | — |
Reaction Steps
10.1 g. of 2-amino-1,3,4-thiadiazole are dissolved in 160 ml. of ethanol, 19.9 g. of α-bromoacetophenone is added and the solution is heated and stirred at reflux for 1 hour. After cooling, the solid is filtered off and dissolved in 750 ml. of water and 40 ml. of 48% hydrobromic acid. This solution is heated at reflux for 1 hour, neutralized by addition of solid ammonium acetate and refluxed 1/2 hour longer. After cooling, the product is collected on a filter, washed with water and dried. The yield of product is 13 g. melting at 127°-130° C. It has the formula: ##STR15##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04419289 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-420c48a2e5f94da09317aa84c11732aa |
| Source note | uspto-grants-1983_12 |