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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925739Generated: October 30, 2026

O-Toluidine → N-(2-Methylphenyl)pyrrolidine

https://huagongshe.com/reaction/1925739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium CarbonateHCID 10340—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN-(2-Methylphenyl)pyrrolidineHCID 14253141.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of o-toluidine (2.0 g; 18.7 mmol) in methanol (62 mL) was added sodium carbonate (4.95 g; 46.75 mmol) followed by 1,4-dibromobutane (4.85 g; 22.4 mmol). The resulting mixture was stirred at 50° C. under a nitrogen atmosphere overnight and then diluted with water and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by automated silica gel column chromatography (Biotage®) eluting with ethyl acetate/hexanes (0 to 40% v/v over 900 mL gradient elution) to yield the title product as a dark yellow-orange oil (1.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178699B2
Source datasetuspto-grants-2012_05
ORD IDord-90640e867e4f4781b5da5988b85986ff
Source noteuspto-grants-2012_05