HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Dimethylphosphonomethylamino)-3-(4-biphenylyl)-propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Dimethyl (aminomethyl)phosphonate | HCID 13310504 | — |
| Reactant | 2-Oxo-3-(4-phenylphenyl)propanoic acid | HCID 13982437 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | 2-(Dimethylphosphonomethylamino)-3-(4-biphenylyl)-propionic acid | HCID 53811687 | — |
Reaction Steps
To a stirred suspension of 4-biphenyl-pyruvic acid in anhydrous THF-EtOH (50 mL, 9:1) is added aminomethylphosphonic acid dimethyl ester (520 mg, 3.7 mmol) in THF-EtOH (5 mL, 9:1). The pH is then adjusted with triethylamine to 6.6. After 20 minutes, sodium cyanoborohydride (100 mg, 1.6 mmol) in THF (2.5 mL) is added over 30 minutes. The solution is stirred for 18 hours and then concentrated. Ether (20 mL) is added and the mixture is cooled and treated with 1N HCl (7 mL). After stirring at room temperature for 30 minutes, the solid is filtered off and washed with ether and water to yield 2-(dimethylphosphonomethylamino)-3-(4-biphenylyl)-propionic acid as a waxy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05294632 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-c5fc5633de0a4753bfdd5e7d70a9820e |
| Source note | uspto-grants-1994_03 |