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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050979Generated: November 1, 2026

Ethyl Acetate → HCID 89533661, compound

https://huagongshe.com/reaction/1050979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Cyclobutene-1,2-dione, 3,4-dimethoxy-HCID 123227—
ReactantHCID 89533660HCID 89533660—
SolventEthanolHCID 702—
ProductHCID 89533661HCID 8953366134%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2.64 g (10 mmol, 1 eq) of methyl (R)-1-(3-amino-2-hydroxybenzoyl)pyrrolidine-2-carboxylate and 2.84 g (20 mmol, 2.0 eq) of 3,4-dimethoxy-3-cyclobutene-1,2-dione in 80 ml of ethanol was heated at 50° C. for four and a half hours. The residue was taken up with ethyl acetate and washed three times with a 1 M aqueous sodium dihydrogen phosphate solution. The organic phase was dried over anhydrous sodium sulfate, filtered and evaporated. The oil was chromatographed on silica gel (300 g prepacked column) eluted with heptane/ethyl acetate (gradient). 1.27 g of methyl (R)-1-[2-hydroxy-3-(2-methoxy-3,4-dioxocyclobut-1-enylamino)benzoyl]pyrrolidine-2-carboxylate were obtained in the form of white solid. Yield=34%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388149B2
Source datasetuspto-grants-2016_07
ORD IDord-f9aab0ffa65b444789ac8173d5e35cb4
Source noteuspto-grants-2016_07