Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374842Generated: October 26, 2026

t-Butyloxycarbonylaspartic acid alpha-benzyl ester → 3-((tert-Butoxycarbonyl)amino)-4-methoxy-4-oxobutanoic acid

https://huagongshe.com/reaction/2374842

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyloxycarbonylaspartic acid alpha-benzyl esterHCID 82036—
ReactantTrimethylsilyldiazomethane hexaneHCID 86587183—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product3-((tert-Butoxycarbonyl)amino)-4-methoxy-4-oxobutanoic acidHCID 14258702—

Reaction Steps

2.0 g (6.18 mmol) of 4-(benzyloxy)-2-[(t-butoxycarbonyl)amino]-4-oxobutanoic acid was dissolved in a solvent mixture of 6 ml of methanol and 12 ml of toluene. 3.7 ml of 2 M trimethylsilyldiazomethane/hexane solution was added to the obtained solution and they were stirred for 3 hours. Additional 0.5 ml of 2 M trimethylsilyldiazomethane/hexane solution was added to the reaction mixture and they were stirred for 1 hour. The solvent was evaporated under reduced pressure. The residue was dissolved in 20 ml of ethanol. 2.0 g of palladium carbon (10% w/v) was added to the obtained solution, and they were stirred in hydrogen gas atmosphere for 19 hours. After the filtration, the solvent was evaporated under reduced pressure to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462630B2
Source datasetuspto-grants-2008_12
ORD IDord-61989a05c92943e49f0e143f902c9deb
Source noteuspto-grants-2008_12