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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045115Generated: October 27, 2026

Ethyl Acetate → Ethyl 1-{[(tert-butoxy)carbonyl]amino}-3-hydroxycyclobutane-1-carboxylate

https://huagongshe.com/reaction/1045115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 3-(Benzyloxy)-1-(Boc-amino)cyclobutanecarboxylateHCID 14728571—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 1-{[(tert-butoxy)carbonyl]amino}-3-hydroxycyclobutane-1-carboxylateHCID 14728572—

Reaction Steps

The 1-(N-(t-butoxycarbonyl)amino)-3-benzyloxy-cyclobutane-1-carboxylic acid ethyl ester synthesized as above is dissolved in an alcohol solvent such as ethanol or an acetate ester solvent such as ethyl acetate ester, and palladium-on-activated carbon (amount: 10 w/w % or more relative to the substrate) is added to the solution in an atmosphere of hydrogen to allow them to react under stirring at room temperature. The reaction solution is then filtered through Celite, and the filtrate is concentrated and purified to yield 1-(N-(t-butoxycarbonyl)amino)-3-hydroxy-cyclobutane-1-carboxylic acid ethyl ester (Step 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563771B2
Source datasetuspto-grants-2013_10
ORD IDord-ad638db0bd574ebd8d6095734348d288
Source noteuspto-grants-2013_10