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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045708Generated: October 29, 2026

Potassium vinyltrifluoroborate → 1-tert-butyl 2-methyl (2S,4R)-4-[(7-methoxy-2-oxo-6-vinyl-1,2-dihydroquinolin-4-yl)oxy]pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/2045708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantHCID 59279885HCID 59279885—
CatalystHCID 178418807HCID 178418807—
SolventEthanolHCID 702—
Product1-tert-butyl 2-methyl (2S,4R)-4-[(7-methoxy-2-oxo-6-vinyl-1,2-dihydroquinolin-4-yl)oxy]pyrrolidine-1,2-dicarboxylateHCID 5927990899.1%

Reaction Steps

Potassium vinyltrifluoroborate (0.913 g, 6.82 mmol), TEA (0.950 mL, 6.82 mmol), and PdCl2(dppf)-CH2Cl2 adduct (0.186 g, 0.227 mmol) were added to a solution of the product from step 2 (2.26 g, 4.54 mmol) in EtOH (45.4 mL). The mixture was then heated to reflux for 1 h. The EtOH was removed in vacuo, and the residue was taken up in EtOAc and extracted with water. The organic layer was dried over MgSO4, and the solvent was removed in vacuo. The crude material was purified on silica gradient elution, 0-5% MeOH/DCM) to yield 2.0 g (99%) of the title compound. LRMS ESI+ ((M-Boc)+H)+345.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08591878B2
Source datasetuspto-grants-2013_11
ORD IDord-f93848d647e94569bf633da037048bff
Source noteuspto-grants-2013_11