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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Styrene | HCID 7501 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4R)-4-(2-bromo-4-chlorophenyl)pyrrolidin-2-one | HCID 66725008 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-((1E)-2-Phenylvinyl)-4-chlorophenyl](4R)pyrrolidin-2-one | HCID 66724933 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344028B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8615d8985e574542ab82005c8f1f2dd7 |
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| Source note | uspto-grants-2013_01 |
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