HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926849Generated: October 30, 2026
Toluene → 4-propyl-1-(1H-pyrrol-1-ylmethyl)pyrrolidin-2-one
https://huagongshe.com/reaction/1926849
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium t-amylate | HCID 23683543 | — |
| Reactant | 1-(Chloromethyl)-4-propylpyrrolidin-2-one | HCID 53629216 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-propyl-1-(1H-pyrrol-1-ylmethyl)pyrrolidin-2-one | HCID 57743102 | 15% |
Reaction Steps
18-Crown-6 (0.158 g, 0.2 eq, 0.6 mmol) is dissolved in absolute ether (20 ml). A 1.7 M solution of potassium tert-amylate in toluene (1.93 ml, 1.1 eq, 3.28 mmol) is added dropwise in a flow of argon. The reaction mixture is stirred for 15 min at room temperature. Pyrrole (0.2 g, 1 eq, 2.98 mmol) is added. The reaction mixture is cooled to −15° C., and a solution of 1-(chloromethyl)-4-propylpyrrolidin-2-one x63 (0.603 g, 1.15 eq, 3.43 mmol) in absolute ether (5 ml) is added dropwise. The resulting solution is stirred for 16 h at 20° C. The contents of the flask are partitioned between 10 ml of water and 30 ml of ethyl acetate. The organic layer is separated. The aqueous one is subjected to additional extraction with ethyl acetate (2×20 ml). The combined extracts are dried with anhydrous Na2SO4 and evaporated. Purification by chromatography on silicagel (dichloromethane/acetone) afford 0.091 g of 4-propyl-1-(1H-pyrrol-1-ylmethyl)pyrrolidin-2-one x264.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183241B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-9819c4c6ae87409baf47678c4ddc5758 |
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| Source note | uspto-grants-2012_05 |
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