HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57404210, compound → HCID 131718642, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57404210 | HCID 57404210 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131718642 | HCID 131718642 | 100% |
Reaction Steps
[1-(Benzyloxycarbonyl)amino-3-methybutyl(methoxy)phosphinyl]acetic acid tert-butyl ester, prepared by the literature procedure: Bartlett, P. A.; Kezer, W. B.; J. Am. Chem. Soc. , 106, 4282 (1984), (357 mg, 0.86 mmol) was dissolved in MeOH (11 mL) and hydrogenolyzed under H2 using 10% Pd/C (84 mg) for approximately one hour. The catalyst was removed by filtration and the solvent removed under reduced pressure to give the title product as an oil (230 mg, 100%). The 300 MHz 1H NMR spectrum was found to be consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05338726 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-8b45a71ca4ca4b42888cf3830ea015a6 |
| Source note | uspto-grants-1994_08 |