Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864562Generated: October 31, 2026

Methyl iodide → N-Methyl-3-nitro-N-(3-pyridinylmethyl)benzamide

https://huagongshe.com/reaction/864562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Nitro-N-(3-pyridinylmethyl)benzamideHCID 743421—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductN-Methyl-3-nitro-N-(3-pyridinylmethyl)benzamideHCID 2211323885.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-nitro-N-(3-pyridylmethyl)benzamide (2.00 g) in tetrahydrofuran (40 ml) was added potassium tert-butoxide (917 mg) in one portion in an ice-cooled bath. The stirring was continued for 40 minutes and then iodomethane (0.53 ml) was added thereto. The reaction mixture was stirred at 0° C. for one hour, then at ambient temperature for five hours. Saturated sodium bicarbonate solution was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated sodium chloride solution. After dried over anhydrous magnesium sulfate and filtered, the solvent was removed in vacuo and the residue was purified by flash chromatography (methanol-chloroform 3%, V/V) to afford 3-nitro-N-methyl-N-(3-pyridylmethyl)benzamide (1.8 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563162
Source datasetuspto-grants-1996_10
ORD IDord-26d477b5f1cd4014bb18bcecf0d83112
Source noteuspto-grants-1996_10