Reacción #74606

Ecuación de reacción

ammonium chloride

Butyl lithium

1-(ethoxymethyl)-1H-pyrazole

hydrochloric acid

2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

→

title compound

Rendimiento 78.0%

1-(Ethoxymethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

Rendimiento 78.0%

Disolventes

tert-butylmethylether

tetrahydrofuran

water

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.WAITat room temperature for 30 minutes
2. 2
   TemperaturaThe mixture was warmed to room temperature
3. 3
   workup.STIRRINGstirred under nitrogen for 60 hours
4. 4
   workup.STIRRINGthe biphasic mixture stirred vigorously for 30 minutes
5. 5
   Extracciónextracted with tert-butylmethylether (3×200.0 mL)
6. 6
   LavadoThe combined organics were washed with saturated aqueous sodium chloride solution (100.0 mL)
7. 7
   workup.STIRRINGstirred with activated charcoal (1 g) for 30 minutes
8. 8
   workup.ADDITIONMagnesium sulphate was added
9. 9
   Filtraciónthe mixture filtered through a pad of Celite™
10. 10
    Lavadowashing with tert-butylmethylether (1 L)
11. 11
    ConcentraciónConcentration in vacuo

Procedimiento

Butyl lithium (2.5 M in hexanes, 32.4 mL, 0.0811 mol) was added slowly via syringe to a solution of 1-(ethoxymethyl)-1H-pyrazole (Preparation 338, 9.3 g, 0.074 mol) in anhydrous tetrahydrofuran (100.0 mL) at 0° C. and stirred under nitrogen for 15 minutes and then at room temperature for 30 minutes. The mixture was cooled to −78° C. and 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (16.5 mL, 0.0811 mol) was added via syringe. The mixture was warmed to room temperature and stirred under nitrogen for 60 hours. Saturated aqueous ammonium chloride solution (50.0 mL) was added followed by water (150.0 mL). The mixture was poured into tert-butylmethylether (200.0 mL) and the biphasic mixture stirred vigorously for 30 minutes. The aqueous layer was acidified to pH 6 with hydrochloric acid (6.0 M aqueous solution) and extracted with tert-butylmethylether (3×200.0 mL). The combined organics were washed with saturated aqueous sodium chloride solution (100.0 mL) and then stirred with activated charcoal (1 g) for 30 minutes. Magnesium sulphate was added and the mixture filtered through a pad of Celite™, washing with tert-butylmethylether (1 L). Concentration in vacuo afforded the title compound as a brown oil, 14.5 g, 78% yield.

Fuente