HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → N-(4-methoxybenzenesulfonyl)-D-valine benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-[4-methoxybenzenesulfonyl]-(D)-valine | HCID 1133588 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-methoxybenzenesulfonyl)-D-valine benzyl ester | HCID 15429254 | 83.6% |
Reaction Steps
To a solution of 2(R)-(4-methoxybenzenesulfonylamino)-3-methylbutyric acid (40 g, 139.2 mmol) and cesium carbonate (85.7 g, 444 mmol) in dimethylformamide was added benzyl bromide (16.1 g, 135 mmol). The reaction mixture was stirred overnight. The dimethylformamide was removed on the rotoevaporator and the residue was dissolved in ethyl acetate (200 ml) and partitioned with an equal volume of water. The organic phase was collected and washed with an equal volume of brine. The aqueous phases were back extracted with ethyl acetate (2×150 ml), combined and dried over magnesium sulfate and condensed to provide 2(R)-(4-methoxybenzenesulfonylamino)-3-methylbutyric acid benzyl ester (42.6 g) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06787559B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-68ce58b2be194aa8a3aee0faad7cbd96 |
| Source note | uspto-grants-2004_09 |