HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049464Generated: October 31, 2026
1-Bromo-2,2-dimethylpropane → HCID 58612135, compound
https://huagongshe.com/reaction/1049464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2,2-dimethylpropane | HCID 12415 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Bromo-2-methoxypyridine | HCID 12533390 | — |
| Catalyst | SIPr | HCID 10883669 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58612135 | HCID 58612135 | — |
Reaction Steps
Under an argon atmosphere, a solution of 1-bromo-2,2-dimethylpropane (14.8 mL) in diethyl ether (120 mL) was added dropwise to magnesium (3.15 g) at a slow refluxing rate. The reaction mixture was heated under reflux for 30 min, and the obtained solution was added dropwise to a solution of 3-bromo-2-methoxypyridine (4.43 g) and PEPPSI™-SIPr (trade name) (805 mg) in THF (80 mL) at room temperature. The reaction mixture was stirred at room temperature for 30 min, and saturated aqueous ammonium chloride solution was added at room temperature. The reaction mixture was extracted with ethyl acetate, and the extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give a crude product of the title compound (4.24 g) as a pale-yellow oil. This compound was used for the next step without further purification.
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-276c3ac8f3554b84a035083cd4b108c5 |
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| Source note | uspto-grants-2016_07 |
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