Reacción #83002

Ecuación de reacción

3,4-epoxy-1-butene

acetic anhydride

tributylamine

acetic acid

→

3,4-diacetoxy-1-butene

Rendimiento 79.0%

Disolventes

diglyme

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe autoclave was purged with nitrogen twice
2. 2
   workup.WAITGC analysis of the crude mixture after 2 hrs revealed

Procedimiento

A 300-mL autoclave was charged with 40 mL (0.50 mol) of 3,4-epoxy-1-butene, 60.0 g (0.59 mol) acetic anhydride, 3.7 g (0.02 mol) of tributylamine, 0.72 g (0.012 mol) acetic acid and 4.2 mL of diglyme. The autoclave was purged with nitrogen twice, then the vessel was pressurized to 8 bars (100 psig) with nitrogen. The agitator was started and an initial sample was taken. The mixture was heated to 125° C. During the course of 2 hrs, samples were taken every 15 min for analysis by GC. GC analysis of the crude mixture after 2 hrs revealed a 79% yield of 3,4-diacetoxy-1-butene with a 90% selectivity and 12% 3,4-epoxy-1-butene. The reaction was observed to be first order in 3,4-epoxy-1-butene with a first order rate constant of 0.017 min-1 (Table A). This example shows the catalytic effect of another tertiary amine with acetic acid as the co-catalyst.

Fuente