Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569206Generated: October 30, 2026

m,alpha-Dichlorotoluene → 3-(2-(3-Chlorophenyl)ethyl)-N-(1,1-dimethylethyl)-2-pyridinecarboxamide

https://huagongshe.com/reaction/569206

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm,alpha-DichlorotolueneHCID 12103—
ReactantSodium BromideHCID 253881—
ReactantN-tert-Butyl-3-methylpyridine-2-carboxamideHCID 5463796—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-(2-(3-Chlorophenyl)ethyl)-N-(1,1-dimethylethyl)-2-pyridinecarboxamideHCID 1412869592%

Reaction Conditions

Temperature-40 °C

Reaction Steps

31.5 g of N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide is dissolved in 600 mL of dry tetrahydrofuran and the resulting solution is cooled to -40° C. Two equivalents of n-butyllithium in hexane are added while the temperature is maintained at -40° C. The solution turned deep purple-red. 1.6 g of sodium bromide is added and the mixture is stirred. A solution of 26.5 g (0.174 mole) m-chlorobenzylchloride in 125 mL of tetrahydrofuran is added while the temperature is maintained at -40° C. The reaction mixture is stirred until the reaction is complete as determined by thin layer chromatography. Water is added to the reaction until the color is dissipated. The reaction mixture is extracted with ethyl acetate, washed with water, and concentrated to a residue. A yield of 92% for the product is shown by chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731447
Source datasetuspto-grants-1988_03
ORD IDord-a2a733ac86704d1a857ca8dfab06ef30
Source noteuspto-grants-1988_03