Reacción #52034

Ecuación de reacción

3,4-di-n-propoxythiophene

1,2,6-hexanetriol

p-toluenesulphonic acid

→

4-(2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.DISTILLATIONDuring this time, 5.8 g of distillate (substantially n-propanol) were collected
2. 2
   workup.ADDITIONThe cooled liquid was diluted with 50 ml of methylene chloride
3. 3
   Lavadowashed to neutrality
4. 4
   Secadothe organic phase was dried over Na2SO4
5. 5
   FiltraciónAfter filtering
6. 6
   Otroevaporating the methylene chloride

Procedimiento

9.06 g (45.2 mmol) of 3,4-di-n-propoxythiophene, 30.3 g (226 mmol) of 1,2,6-hexanetriol and 0.09 g (0.5 mmol) of p-toluenesulphonic acid are heated to 150 to 165° C. (bath temperature) under N2 for 3 h. During this time, 5.8 g of distillate (substantially n-propanol) were collected. The cooled liquid was diluted with 50 ml of methylene chloride, washed to neutrality and to free it of hexanetriol with water and the organic phase was dried over Na2SO4. After filtering and evaporating the methylene chloride, the residue (6.73 g=74.8% of theory) was identified by 1H NMR spectroscopy (in CDCl3 against TMS) using δ=6.30 ppm (2H, thiophene H) and 2.85 ppm (1H, OH) as being substantially 4-(2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)-1-butanol.

Fuente