Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505042Generated: October 31, 2026

Toluene → 4-Methyl-3-(5-methylpyridin-2-yl)aniline

https://huagongshe.com/reaction/1505042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-5-methyl-pyridineHCID 581393—
Reactant4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 16086089—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product4-Methyl-3-(5-methylpyridin-2-yl)anilineHCID 57493281—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a round-bottom flask containing 5-amino-2-methyl-phenylboronic acid pinacol ester (348 mg, 1.5 mmol), 2-chloro-5-methylpyridine (381 mg, 3 mmol), Pd(PPh3)4 (192 mg, 0.15 mmol) is added toluene (12 ml), EtOH (3 ml) and 2M aqueous Na2CO3 solution (3 ml). The flask is purged with argon and sealed. The mixture is stirred at 90° C. for 18 hours, cooled to room temperature and then water (20 ml) and ethyl acetate (20 ml) are added. The organic layer is separated, washed with brine, dried over MgSO4 and concentrated. The residue is purified by silica gel flash chromatography, eluted with 2% methanol in dichloromethane to afford 4-Methyl-3-(5-methylpyridin-2-yl)aniline as a brown oil. LC-MS m/z: 199.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216964B2
Source datasetuspto-grants-2015_12
ORD IDord-152bcdb22cd045f197c7bb75dcecb770
Source noteuspto-grants-2015_12