HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219673Generated: October 25, 2026
Rolziracetam → 5-(3-Oxo-4-phenyl-butyl)-pyrrolidin-2-one
https://huagongshe.com/reaction/2219673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Rolziracetam | HCID 71893 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(3-Oxo-4-phenyl-butyl)-pyrrolidin-2-one | HCID 12970083 | 70.9% |
Reaction Steps
To a solution of tetrahydro-pyrrolizine-3,5-dione (5 g, 36 mmol) in CH2Cl2 (320 mL) at 0° C. was added benzyl magnesium chloride (1M solution in THF, 39 mL, 39 mmol) dropwise. The solution was stirred at 0° C. for 3 h and was quenched with saturated aqueous ammonium chloride. After warming to room temperature, the aqueous solution was extracted with CH2Cl2 (3×). The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by medium pressure chromatography eluting with a solvent gradient (1% MeOH in CH2Cl2 to 2% MeOH in CH2Cl2) to yield 5.9021 g of 5-(3-oxo-4-phenyl-butyl)-pyrrolidin-2-one. 1H NMR (CDCl3) δ 87.35-7.18 (m, 5H), 3.69 (s, 2H), 3.56 (m, 1H), 2.50 (t, 2H), 2.27 (m, 2H), 2.15 (m, 1H), 1.73 (m, 2H), 1.61 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414071B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-a473c6ac8b3448c89261acd40656a5df |
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| Source note | uspto-grants-2008_08 |
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