HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl (2S)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-benzyloxycarbonyl-DL-3-phenylalanine | HCID 100081 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl (2S)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoate | HCID 11438389 | 101% |
Reaction Steps
To a solution of N-benzyloxycarbonyl-DL-phenylalanine (155 g, 0.518 mol) in DMF (800 mL) were added mortar-pulverized potassium hydrogencarbonate (104 g, 1.04 mol) and methyl iodide (53 mL, 0.86 mol), and the mixture was stirred at room temperature for 5 hours. This reaction mixture was added to water (1800 mL) and extracted with ethyl acetate-hexane (4:1). The extract was washed successively with 2 portions of water (500 mL each), 5% sodium sulfite aqueous solution (500 ml) and saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give 164 g (100%) of N-benzyloxycarbonyl-DL-phenylalanine methyl ester as a colorless clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528514B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-3b64b3b89ca7460db05d0210f68263dd |
| Source note | uspto-grants-2003_03 |