HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 54393443, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 3779431 | HCID 3779431 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54393443 | HCID 54393443 | — |
Reaction Steps
A solution of 37.4 g of 2-amino-6-methyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester and 6.8 g of sodium ethylate in 500 ml of ethanol is brought to the boil and treated with 17.1 g of benzyl bromide. After boiling for a further 60 minutes under reflux, the mixture is concentrated by distillation and the residue is taken up in 300 ml of chloroform and extracted by shaking twice with 100 ml of water. Concentration of the organic phase and recrystallization from ethanol gave 2-amino-3-benzyl-6-methyl-4-(3'-nitrophenyl)-3,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester of melting point 208° C (29.4 g, 63% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002762 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-434d1d6ffc244f68a69bbca788bbaddf |
| Source note | uspto-grants-1977_01 |