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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2,2-dimethylpropane | HCID 12415 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Chloro-3-(2-fluoro-5-methoxyphenyl)-6-methoxypyridine | HCID 117760023 | — |
| Catalyst | SIPr | HCID 10883669 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Fluoro-5-methoxyphenyl)-6-methoxy-2-neopentylpyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382188B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-f55c46a76d934468a25155967e9e418f |
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| Source note | uspto-grants-2016_07 |
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