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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389212Generated: October 31, 2026

Water → 1-t-Butyl 2-methyl (2S,4R)-4-[(7-methoxy-3-vinylquinolin-2-yl)oxy]pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/389212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantHCID 59287096HCID 59287096—
CatalystCID 53485975HCID 53485975—
SolventEthanolHCID 702—
Product1-t-Butyl 2-methyl (2S,4R)-4-[(7-methoxy-3-vinylquinolin-2-yl)oxy]pyrrolidine-1,2-dicarboxylateHCID 59287274—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-t-butyl 2-methyl (2S,4R)-4-[(3-bromo-7-methoxyquinolin-2-yl)oxy]pyrrolidine-1,2-dicarboxylate (2.0 g, 4.2 mmol) in EtOH (30 mL), TEA (0.87 mL, 6.23 mmol) was added. Potassium vinyltrifluoroborate (0.84 g, 6.23 mmol) and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.17 g, 0.21 mmol) were then added, and the reaction mixture was stirred at 100° C. for 2 hours. The reaction mixture was worked up with EtOAc and H2O, and the layers were separated. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The crude material was purified on silica (gradient elution, 0-40% EtOAc/hexanes) to yield the title compound as an oil. LRMS (M+H-tBu)+=373.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377874B2
Source datasetuspto-grants-2013_02
ORD IDord-89f7089090734751a9c3427e9ec79281
Source noteuspto-grants-2013_02