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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPyrroleHCID 8027—
Reactant18-Crown-6HCID 28557—
ReactantPotassium t-amylateHCID 23683543—
Reactant1-(Chloromethyl)-4-propylpyrrolidin-2-oneHCID 53629216—
SolventDiethyl EtherHCID 3283—
Product4-propyl-1-(1H-pyrrol-1-ylmethyl)pyrrolidin-2-oneHCID 5774310215%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183241B2
Source datasetuspto-grants-2012_05
ORD IDord-9819c4c6ae87409baf47678c4ddc5758
Source noteuspto-grants-2012_05