HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → N-hydroxy-2-[[methyl phenylphosphinyl](2-phenylethyl)-amino]-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | n-(Methylphenylphosphinyl)-n-(2-phenylethyl)glycine methyl ester | HCID 10806391 | — |
| Reactant | HCID 178514655 | HCID 178514655 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-hydroxy-2-[[methyl phenylphosphinyl](2-phenylethyl)-amino]-acetamide | HCID 10830393 | — |
Reaction Steps
N-(Methylphenylphosphinyl)-N-(2-phenylethyl)glycine methyl ester (300 mg, 0.905 mmol) is treated with 0.77 mL of NH2OK (1.76M in methanol, solution prepared as described in Fieser and Fieser, Vol. 1, p. 478). The mixture is stirred for 3 hours at room temperature, neutralized with formic acid and concentrated. The crude product is purified by silica gel flash chromatography (85:15 ethyl acetate:ethanol) giving the product with slight impurities. Preparative TLC (90:10 ethyl acetate:ethanol) gives N-hydroxy-2-[[methyl phenylphosphinyl](2-phenylethyl)-amino]-acetamide as a colorless solid: MS-IS m/z 333 [M+H]+, 350 [M+NH4 ]+, 355 [M+Na]+, 371 [M+K]+. (R1 =phenyl ethyl, R2 =H, R3 =methyl, R4 =phenyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05830915 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-d231838717394c229e3e81149e730383 |
| Source note | uspto-grants-1998_11 |