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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799190Generated: November 1, 2026

Styrene → 4-[2-((1E)-2-Phenylvinyl)-4-chlorophenyl](4R)pyrrolidin-2-one

https://huagongshe.com/reaction/1799190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyreneHCID 7501—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
Reactant(4R)-4-(2-bromo-4-chlorophenyl)pyrrolidin-2-oneHCID 66725008—
Catalystpalladium(II) acetateHCID 167845—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
Product4-[2-((1E)-2-Phenylvinyl)-4-chlorophenyl](4R)pyrrolidin-2-oneHCID 6672493379%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of (4R)-4-(2-bromo-4-chlorophenyl)pyrrolidin-2-one (140 mg, 0.51 mmol), Pd(OAc)2 (34 mg, 0.15 mmol) and triphenylphosphine (0.3 mmol) in DMF (1 mL) was added styrene (0.17 mL, 2 mmol) followed by diisopropylethylamine (0.17 mL, 1.02 mmol) under a N2 atmosphere. The reaction mixture was heated to 90° C. overnight. The mixture was then cooled to room temperature and diluted with 1N HCl aq. solution (10 mL) and extracted with ethyl acetate (3×30 mL). The combined organic phases were washed with brine (3×30 mL) and dried over MgSO4. The solvent was removed in vacuo to provide 4-[2-((1E)-2-phenylvinyl)-4-chlorophenyl](4R)pyrrolidin-2-one (3a) (120 mg). MS (ESI) m/z 284.02 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344028B2
Source datasetuspto-grants-2013_01
ORD IDord-8615d8985e574542ab82005c8f1f2dd7
Source noteuspto-grants-2013_01