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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233031Generated: October 25, 2026

Potassium Carbonate → 2-(3-Methoxyphenyl)-1-(2-pyridinylmethyl)pyrrolidine

https://huagongshe.com/reaction/233031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPicolyl chloride hydrochlorideHCID 23392—
Reactant2-(3-Methoxyphenyl)pyrrolidineHCID 3613824—
SolventAcetonitrileHCID 6342—
Product2-(3-Methoxyphenyl)-1-(2-pyridinylmethyl)pyrrolidineHCID 2336126391%

Reaction Steps

To a solution of 2-(3-methoxyphenyl)pyrrolidine (3.0 g) in dry acetonitrile (70 ml) was added milled potassium carbonate (6.1 g) followed by 2-picolyl chloride hydrochloride (3.1 g) at ambient temperature, under nitrogen, with stirring for 65 hrs. The reaction mixture was filtered through a pad of celite, and the filter cake was washed with ethyl acetate. The combined filtrates were concentrated and the residue was purified by flash column chromatography (silica gel, 5% methanol/ether). The appropriate fractions were collected and concentrated to give 4.1 g (91%) of 2-(3-methoxyphenyl)-1-(2-pyridinylmethyl)pyrrolidine. 2-(3-Methoxyphenyl)-1-(2-pyridinylmethyl)pyrrolidine and 48% hydrobromic acid (40 ml) were warmed to 100° C. for 7 hrs, cooled to ambient temperature, and neutralized with saturated sodium bicarbonate solution. The mixture was extracted with dichloromethane (2 times). The combined organic extracts were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by flash column chromatography (silica gel, 1:1 ethyl acetate/dichloromethane). The appropriate fractions were collected and concentrated to give 2.7 g (69%) of product, mp 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591856
Source datasetuspto-grants-1997_01
ORD IDord-abe4dc7be5dd4f3c986db96eb8435d7e
Source noteuspto-grants-1997_01