Reacción #84718

Ecuación de reacción

(4S,5S)-5-amino-2,2-dimethyl-tetrahydro-2H-pyran-4-ol

triethylamine

dioxane

2-(trimethylsilyl)ethyl 2,5-dioxopyrrolidine-1-carboxylate

→

title compound

Rendimiento 86.4%

2-(trimethylsilyl)ethyl (3S,4S)-4-hydroxy-6,6-dimethyl-tetrahydro-2H-pyran-3-ylcarbamate

Rendimiento 86.4%

Disolventes

water

ethyl acetate

Condiciones de reacción

Tratamiento posterior

1. 1
   Lavadowashed with brine
2. 2
   OtroThe organic layer was separated
3. 3
   Concentraciónconcentrated
4. 4
   OtroThe resulting residue was purified by silica gel chromatography

Procedimiento

To a solution of (4S,5S)-5-amino-2,2-dimethyl-tetrahydro-2H-pyran-4-ol (1.1 g, 4.0 mmol) and triethylamine (1.1 mL, 8.0 mmol) in a mixed solvent of dioxane (5 mL) and water (5 mL) at room temperature was added 2-(trimethylsilyl)ethyl 2,5-dioxopyrrolidine-1-carboxylate (1.2 g, 4.8 mmol). The reaction mixture was stirred at room temperature for 4 hours. After that, the solution was diluted with ethyl acetate and washed with brine. The organic layer was separated and concentrated. The resulting residue was purified by silica gel chromatography using petroleum ether/ethyl acetate=4/1 to 1/1 as the eluent to afford the title compound (1.0 g, 86% for 2 steps) as a yellow oil.

Fuente