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, andd 100 milliliters of ethanol were mixed, heated to reflux, and refluxed for 1 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-imadazo (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 | US04054573 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-88e1b7c4da51499eadc8b374563a6c59 |
| Source note | uspto-grants-1977_10 |