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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049391Generated: November 2, 2026

1-Bromo-2,2-dimethylpropane → 3-(2-Fluoro-5-methoxyphenyl)-6-methoxy-2-neopentylpyridine

https://huagongshe.com/reaction/1049391

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2,2-dimethylpropaneHCID 12415—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant2-Chloro-3-(2-fluoro-5-methoxyphenyl)-6-methoxypyridineHCID 117760023—
CatalystSIPrHCID 10883669—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Fluoro-5-methoxyphenyl)-6-methoxy-2-neopentylpyridineHCID 117760134—

Reaction Steps

Under an argon atmosphere, a solution of 1-bromo-2,2-dimethylpropane (9.82 mL) in diethyl ether (100 mL) was added dropwise to magnesium (1.72 g) at a slow refluxing rate, and the reaction mixture was heated under reflux further for 1 hr. Under an argon atmosphere, the obtained solution was added dropwise to a solution of 2-chloro-3-(2-fluoro-5-methoxyphenyl)-6-methoxypyridine (3.79 g) and a PEPPSI™-SIPr catalyst (trade name) (970 mg) in THF (70 mL) at room temperature, and the mixture was stirred at room temperature for 15 min. To the reaction mixture was added saturated aqueous ammonium chloride solution at room temperature, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (3.97 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-f55c46a76d934468a25155967e9e418f
Source noteuspto-grants-2016_07