HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S)-2-amino-2-phenylpropanoic acid → (S)-2-(Boc-amino)-2-phenylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S)-2-amino-2-phenylpropanoic acid | HCID 853461 | — |
| Reactant | Carbonic acid, bis(1,1-dimethylethyl) ester | HCID 10219638 | — |
| Reactant | Trimethylazanium hydroxide | HCID 11446287 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-2-(Boc-amino)-2-phenylpropanoic acid | HCID 13678038 | — |
Reaction Steps
To a suspension of 500 mg of 2-phenyl-D-alanine (3.02 mmol) and trimethylammonium hydroxide (aqueous solution 10%, 2.8 mL, 3.02 mmol) in 15 mL of acetonitrile, diterbutylcarbonate (1.047 g, 4.8 mmol) was added and the mixture was stirred at room temperature for 2 days. The solvent was then removed under vacuo, the residue was dissolved in water and washed with diethylether. The aqueous layer was acidified to pH=3-4 with citric acid and the product was extracted with ethyl acetate (3×20 mL). The combined organic phase was washed with water, dried over Na2SO4 and evaporated. The title product was recovered as white solid (630 mg, yield 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541429B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-fb4951d7af0d4849878154799b7a4aa2 |
| Source note | uspto-grants-2013_09 |