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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368969Generated: October 30, 2026

1-Bromo-3-chlorobenzene → HCID 10869200, compound

https://huagongshe.com/reaction/368969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chlorobenzeneHCID 7928—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-6-methylnicotinic acidHCID 121724—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10869200HCID 1086920044.3%

Reaction Steps

Magnesium (4.8 g, 200 mmol) was added to a tetrahydrofuran (400 ml) solution of 3-bromochlorobenzene (38 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 (9.2 g, 53 mmol) and then stirred overnight 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 (chloroform) to give 2-chloro-3-(3-chlorobenzoyl)-6-methylpyridine (6.25 g, 44%) as an oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136810
Source datasetuspto-grants-2000_10
ORD IDord-4db5afa776854204a37080e4cd08ba4c
Source noteuspto-grants-2000_10