HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → (R)-benzyl 2-((tert-butoxycarbonyl)amino)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (2R)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoic acid | HCID 637605 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-benzyl 2-((tert-butoxycarbonyl)amino)-3-methylbutanoate | HCID 11243734 | 98.6% |
Reaction Steps
N-Tert-butoxycarbonyl-D-valine (70 g, 0.32 mol) and cesium carbonate (200.2 g, 0.615 mol) were stirred in dry dimethylformamide (550 mL). Benzyl bromide (40.32 mL, 0.336 mol) was added and the reaction mixture was stirred overnight. The material was concentrated on the roto-evaporator and the residue was dissolved in methylene chloride (200 mL) and the methylene chloride layer was washed with water and brine, dried over magnesium sulfate and concentrated to give N-tert-butoxycarbonyl-D-valine benzyl ester (97 g) as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492394B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-7d7c86b2a22b4ddc92f881785dfab1b5 |
| Source note | uspto-grants-2002_12 |