HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 20359956, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Hydroxyfluromidine | HCID 3082418 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20359956 | HCID 20359956 | — |
Reaction Steps
1-Hydroxy-6-chloro-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine (5 grams), 10 milliliters of benzyl bromide, 20 grams of anhydrous potassium carbonate, and 100 milliliters of ethanol were mixed, heated to reflux, and refluxed for one hour. The reaction mixture was then filtered, evaporated under vacuum, and extracted with diethyl ether. The extract was filtered and evaporated under vacuum yielding a dark oil which on standing crystallized as the desired 1-benzyloxy-6-chloro-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine. It was recrystallized from a mixture of acetone and petroleum ether boiling at 60°-80° C., m.p., 107°-09° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04000145 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-ee18e8f7a8f9456a9b9435df4c557c19 |
| Source note | uspto-grants-1976_12 |