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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368971Generated: October 29, 2026

3-Bromotoluene → HCID 11053930, compound

https://huagongshe.com/reaction/368971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromotolueneHCID 11560—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-6-methylnicotinic acidHCID 121724—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11053930HCID 1105393052.1%

Reaction Steps

Magnesium (4.82 g, 200 mmol) was added to a tetrahydrofuran (300 ml) solution of 3-bromotoluene (35.1 g, 200 mmol), and the mixture was stirred at room temperature. Since spontaneous exothermic reaction occurred, the stirring was continued until the exothermicity was ceased. The reaction solution was cooled to -40° C., mixed with 2-chloro-6-methylnicotinic acid (11.6 g, 68 mmol) and then stirred for 16 hours at room temperature. The reaction solution was mixed with saturated ammonium chloride aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was removed by filtration and then the filtrate was concentrated under a reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 2-chloro-6-methyl-3-(3-methylbenzoyl)pyridine (8.70 g, 52%) as a pale yellow oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136810
Source datasetuspto-grants-2000_10
ORD IDord-894023bd3d4e4540a4ee07cdb672db17
Source noteuspto-grants-2000_10