HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorobenzyl chloride → HCID 12219984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | HCID 796646 | HCID 796646 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12219984 | HCID 12219984 | — |
Reaction Steps
To a solution of 6.6 g of potassium hydroxide (85%) and 10.3 g of sodium bromide in 100 ml of water and 150 ml of methanol is added, in portions, 17.6 g of 9-hydroxy-2-methyl-4H-pyrido[ 1,2-a]pyrimidin-4-one and the mixture stirred for 0.25 hours. To this is then added 19.6 g of 2,4-dichlorobenzyl chloride dissolved in 50 ml of 95% ethanol and the mixture stirred and refluxed for about 6 hours. The mixture is concentrated to dryness in vacuo and the residue is distributed between 500 ml of chloroform and 250 ml of water. Workup of the chloroform solution yields 9-[ (2,4-dichlorobenzyl)oxy]-2-methyl-4H-pyrido[ 1,2-a]-pyrimidin-4-one, m.p. 180°-182° after recrystallization from acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04022897 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-4abf0794ded047fe98ec47b00d4e39d2 |
| Source note | uspto-grants-1977_05 |