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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112283Generated: November 1, 2026

Methane → (2S)-2-[[(2S)-1-ethoxy-1-oxopentan-2-yl]amino]propanoic acid

https://huagongshe.com/reaction/2112283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantN-[(S)-1-Carbethoxybutyl]-(S)-alanine Benzyl EsterHCID 11493275—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
Product(2S)-2-[[(2S)-1-ethoxy-1-oxopentan-2-yl]amino]propanoic acidHCID 1001515959.5%

Reaction Steps

A solution of N-[1-(S)-ethoxycarbonyl-1-butyl]-(S)-alanine benzyl ester (14.5 g, as obtained in Step-I) in ethanol (150 ml) was hydrogenated in the presence of 10% palladised charcoal (0.8 g) under 40-45 psi hydrogen pressure for 1.5 to 2 hrs. The reaction mixture was concentrated under reduced pressure to give an oil. Crystallization from a mixture of acetonitrile and ethanol (1:3) gave 6.1 g the title compound

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521566B2
Source datasetuspto-grants-2009_04
ORD IDord-2179f9431586465fb002439e8133d5d0
Source noteuspto-grants-2009_04