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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009464Generated: October 26, 2026

3-Chloro-2-methylaniline → N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)glycinamide

https://huagongshe.com/reaction/1009464

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methylanilineHCID 6894—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-N-(4-methoxybenzyl)acetamideHCID 46736691—
SolventDimethylformamideHCID 6228—
ProductN2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)glycinamideHCID 2641749365.9%

Reaction Steps

3.93 g of 3-chloro-2-methylaniline was dissolved in 10 mL of DMF, and 2.00 g of potassium carbonate was added thereto, followed by portionwise addition of 3.55 g of 2-bromo-N-(4-methoxybenzyl)acetamide over 1 hour. The mixture was stirred at room temperature overnight, and ice water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=70:30 to 30:70) to obtain 2.89 g of N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)glycinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973078B2
Source datasetuspto-grants-2011_07
ORD IDord-487d1c7550d14bbda2bcd20b348ee1ee
Source noteuspto-grants-2011_07