HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-[4-methoxybenzenesulfonyl]-alanine methyl ester | HCID 7081982 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate | HCID 22907154 | — |
Reaction Steps
To a suspension of sodium hydride (0.60 g, 11.0 mmol) in dimethylformamide (20.0 mL), is added N-[4-methoxybenzenesulfonyl]-alanine methyl ester (2.6 g, 10.0 mmol) in dimethylformamide (10.0 mL). After stirring at room temperature for 30 minutes, benzyl bromide (1.22 mL, 10.0 mmol) is added, and the reaction is stirred for two hours at room temperature. The reaction is then partitioned between ether and brine, the organic layer is dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (20% ether/hexanes) to give methyl 2-[[4-methoxybenzenesulfonyl]-(benzyl)amino]-propionoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646167 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-c9a5b98f988f4afc8ad6f62b26af50be |
| Source note | uspto-grants-1997_07 |