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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274240Generated: November 4, 2026

Triethylamine → 1-(4-bromo-3-methylphenyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1274240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-3-methylanilineHCID 23359—
Reactant4-Chlorobutyryl chlorideHCID 78370—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(4-bromo-3-methylphenyl)pyrrolidin-2-oneHCID 1121899889.8%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A stirred solution of 4-bromo-3-methylaniline (50.3 g, 0.27 mole) and triethylamine (41.4 ml, 0.30 mole) in THF (250 ml) at 0° C. under argon was treated dropwise with 4-chlorobutyryl chloride (33.4 ml, 0.30 mole). The mixture was stirred for 1 hour at 0-5° C., then potassium t-butoxide (82.5 g, 0.74 mole) was added portionwise over 20 minutes, maintaining temperature below 25° C. The reaction mixture was stirred at 25° C. for a further 2.5 hrs, then treated with water (100 ml), followed after 0.25 hrs with 10% Na2CO3 solution and then extracted with ethyl acetate. The extract was washed with water, dil. HCl acid, then brine, dried (Na2SO4) and concentrated in vacuo to afford the title compound as a pale yellow solid (61.6 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156783
Source datasetuspto-grants-2000_12
ORD IDord-6466ea30aa7943e883d5bfea90230882
Source noteuspto-grants-2000_12