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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388225Generated: October 31, 2026

Potassium vinyltrifluoroborate → 1-t-Butyl 2-methyl (2S,4R)-4-{[(4-vinyl-1,3-dihydro-2H-isoindol-2-yl)carbonyl]oxy}pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/388225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Reactant1-(1,1-Dimethylethyl) 2-methyl (2S,4R)-4-(((4-bromo-1,3-dihydro-2H-isoindol-2-yl)carbonyl)oxy)-1,2-pyrrolidinedicarboxylateHCID 53465566—
SolventEthanolHCID 702—
SolventPotassium bisulfateHCID 516920—
Product1-t-Butyl 2-methyl (2S,4R)-4-{[(4-vinyl-1,3-dihydro-2H-isoindol-2-yl)carbonyl]oxy}pyrrolidine-1,2-dicarboxylateHCID 45378372—

Reaction Steps

To a solution of 1-t-butyl 2-methyl (2S,4R)-4-{[(4-bromo-1,3-dihydro-2H-isoindol-2-yl)carbonyl]oxy}pyrrolidine-1,2-dicarboxylate (10.0 g, 21.3 mmol) in EtOH (200 mL) was added potassium vinyltrifluoroborate (4.28 g, 32 mmol) and Et3OH (4.5 mL, 32 mmol) followed by dichloro[1,1-bis(diphenylphosphino)ferrocene]palladium (II) chloride dichloromethane adduct (175 mg, 0.21 mmol). The reaction mixture was heated to reflux for 6 hours, cooled to RT, diluted with 10% aqueous KHSO4. The EtOH was removed by evaporation in vacuo. The aqueous residue was extracted with EtOAc, and the organic phase washed with brine, dried over Na2SO4. The solvent was evaporated, and the crude product was purified by chromatography on silica eluting with 40-60% EtOAc/hexane to give, after evaporation, the title compound (8.18 g). LRMS (ESI) m/z 417.2 [(M+H)+; calcd for C22H29N2O6: 417.2].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377873B2
Source datasetuspto-grants-2013_02
ORD IDord-7c911949435d4d8d83d30d6c387581fb
Source noteuspto-grants-2013_02