HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → 2-(4-Bromobenzyl)-4-(4-bromophenyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 59104-21-1 | HCID 5020713 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Bromobenzyl)-4-(4-bromophenyl)pyrimidine | HCID 21476409 | 154.7% |
Reaction Steps
To a stirred mixture of 4-bromophenyl-acetamidine (11.25 g, 0.04 mole) and 1-dimethylamino-3-dimethylimonio-1-(4-bromophenyl)-1-propane perchlorate (15.25 g, 0.04 mole) in 100 mL of dry ethanol is added 0.04 mole sodium ethoxide (prepared from 0.92 g Na and 65 mL ethanol). After stirring for 30 min at room temperature a further equivalent of sodium ethoxide is added, and the mixture is heated under reflux for 2 hr. The solvent is removed under reduced pressure, and the yellow-brown residue triturated with 150 mL water. The solid is filtered, washed with water, dried in air and recrystallized from ether:hexane (1:3) to give 12.5 g (77%) of a pale yellow crystalline solid, mp 93°-94° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05606058 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-a3febe43b46e408db115550da443b1ff |
| Source note | uspto-grants-1997_02 |