Reaktion #6438

Reaktionsgleichung

4,6-Bis(1,1-dimethylethyl) 5 hydroxy-2-methyl pyrimidine

sodium hydride

2-Methoxyethoxymethyl chloride

→

crude product

4,6-Bis(1,1-dimethylethyl)-5-[(2 methoxyethoxy)methoxy]-2-methylpyrimidine

Lösungsmittel

tetrahydrofuran

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe reaction is quenched by the addition of saturated ammonium chloride
2. 2
   Sonstigethe tetrahydrofuran is evaporated
3. 3
   ExtraktionThe organics are extracted into 300 mL of ether
4. 4
   WaschenThe ether is washed with 100 mL of brine
5. 5
   Trocknendried over magnesium sulfate
6. 6
   SonstigeEvaporation of the solvent

Vorschrift

4,6-Bis(1,1-dimethylethyl) 5 hydroxy-2-methyl pyrimidine (9.8 g, 44.1 mmoles) is dissolved in 100 mL of tetrahydrofuran and added dropwise to a suspension of sodium hydride (1.2 g, 48.5 mmoles) in THF (50 mL) at 0° C. The reaction mixture is warmed to room temperature over 15 minutes. 2-Methoxyethoxymethyl chloride (7.1 g, 57.3 mmoles) is added to the reaction mixture at room temperature. After being stirred at room temperature for 4 hours, the reaction is quenched by the addition of saturated ammonium chloride and the tetrahydrofuran is evaporated. The organics are extracted into 300 mL of ether. The ether is washed with 100 mL of brine and dried over magnesium sulfate. Evaporation of the solvent gives the crude product which is purified by flash chromatography (silica, 10% ether/hexane). Yield of 4,6 bis(1,1-dimethylethyl)-5-[(2-methoxyethoxy)methoxy]-2-methylpyrimidine=11.3 g (82%) as a clear oil.

Quelle