HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 71184307, compound → (3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 71184307 | HCID 71184307 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic Acid | HCID 7146283 | 93.2% |
Reaction Steps
To a solution of 3 g (S)-methyl 3-(dibenzylamino)-4-oxo-4-(2,4,5-trifluorophenyl)butanoate in 100 ml ethanol, was added 0.5 g of 10% Pd/C under an atmosphere of nitrogen. The atmosphere of nitrogen was replace with an atmosphere of hydrogen, and the reaction was carried out at 25° C. for 5 h. After completion of the reaction, the reaction mixture was filtered through diatomite. The filtrate was concentrated, and the pH was adjusted to 5˜6 by addition of 10% hydrochloric acid. The aqueous layer was washed with ethyl acetate, and then concentrated to obtain 1.47 g (R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic acid as white solid, with a yield of 93.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710255B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-de50ab816e0c4d68989df5f69d129144 |
| Source note | uspto-grants-2014_04 |