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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323134Generated: October 25, 2026

O-Toluidine → N-Benzyl-o-toluidine

https://huagongshe.com/reaction/323134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-Benzyl-o-toluidineHCID 7940243.2%

Reaction Steps

To a solution of 2-methylaniline (1.0 g) and triethylamine (0.95 g) in N,N-dimethylformamide (15 ml) was added benzyl bromide (1.9 g) at ambient temperature and the mixture was stirred at ambient temperature overnight. The reaction mixture was diluted with ethyl acetate and it was washed with water and brine. Drying, filtering and the removal of solvents afforded a crude product. The crude product was chromatographed on silica gel (n-hexane:ethyl acetate=10:1) to give N-benzyl-2-methylaniline (795 mg) as a slightly yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211242B1
Source datasetuspto-grants-2001_04
ORD IDord-05f846309ebb430c9ce70a7852c1dbbf
Source noteuspto-grants-2001_04