1-Bromo-2,2-dimethylpropane → HCID 58612135, compound

HRID 1049464Notes

Reaction equation

HRID 1049464 reaction equation
Br[CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4].[Mg].Br[C:9]1[C:10]([O:15][CH3:16])=[N:11][CH:12]=[CH:13][CH:14]=1.[Cl-].[NH4+]>C(OCC)C.C1COCC1.CC(C1C=CC=C(C(C)C)C=1N1[C-]=[N+](C2C(C(C)C)=CC=CC=2C(C)C)CC1)C>[CH3:16][O:15][C:10]1[C:9]([CH2:2][C:3]([CH3:6])([CH3:5])[CH3:4])=[CH:14][CH:13]=[CH:12][N:11]=1

Participants

8

Procedure

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.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureunder reflux for 30 min
  3. extractionThe reaction mixture was extracted with ethyl acetate
  4. washthe extract was washed with water and saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-276c3ac8f3554b84a035083cd4b108c5
Source dataset
uspto-grants-2016_07
Patent number
US09382188B2

Reaction notes

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