HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 12354099, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 12354095 | HCID 12354095 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12354099 | HCID 12354099 | — |
Reaction Steps
To a solution of 6.1 g. of 2,3-dihydro-5-hydroxycyclopenta[d]pyrido[1,2-a]pyrimidin-10(1H)-one in 100 ml of N,N-dimethylformamide is added, portionwise, a total of 1.6 g of a 50% dispersion of sodium hydride in mineral oil. A yellow precipitate of the sodium salt separates. The mixture is allowed to stir for 0.5 hour at room temperature, and then 6.2 g. of benzyl bromide dissolved in 25 ml of N,N-dimethylformamide is added, dropwise, followed by 100 mg. of copper bronze powder. The mixture is stirred and heated to 100°-110° and kept at that temperature for 2 hours. The hot solution is filtered, concentrated in vacuo, and the solid residue recrystallized from cyclohexane to give 7.2 g. of product, m.p. 150°-152°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03965100 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-1728dd7f4fdd4829b924ed95071b3c4e |
| Source note | uspto-grants-1976_06 |