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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742205Generated: November 1, 2026

HCID 57404210, compound → HCID 131718642, compound

https://huagongshe.com/reaction/1742205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57404210HCID 57404210—
SolventMethanolHCID 887—
ProductHCID 131718642HCID 131718642100%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338726
Source datasetuspto-grants-1994_08
ORD IDord-8b45a71ca4ca4b42888cf3830ea015a6
Source noteuspto-grants-1994_08