Reacción #5248

Ecuación de reacción

sulfuric acid

1,4-dichloro-2,3-butanediol

trioxane

1,4-dichloro-2,3-butanediol

→

4,5-Dichloromethyl-1,3-dioxolane

Rendimiento 89.5%

Disolventes

1,2-dichloroethane

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroA three-neck 500-mL flask equipped with a thermometer, a mechanical stirrer, an addition funnel, a condenser
2. 2
   workup.ADDITIONDuring the addition period
3. 3
   Otrothe flask was immersed in an ice bath
4. 4
   Temperaturato maintain the reaction temperature at 21.5° C. to 25.5° C. for 2.1 hours
5. 5
   OtroThe acid layer was removed
6. 6
   Lavadowashed once with 30 mL EDC
7. 7
   OtroThe combined EDC solutions were quenched with 2% NaHCO3 (600 mL)
8. 8
   Lavadowashed with deionized water (400 mL), 1% NaHCO3 solution (400 mL), deionized water (400 mL

Procedimiento

A three-neck 500-mL flask equipped with a thermometer, a mechanical stirrer, an addition funnel, a condenser, and a positive nitrogen atmosphere was charged with 1,4-dichloro-2,3-butanediol (50.0 g, 0.314 mole), trioxane (9.43 g, 0.314 mole), and 1,2-dichloroethane (EDC) (300 mL). The 1,4-dichloro-2,3-butanediol was not totally dissolved. Concentrated sulfuric acid (46.3 g, 0.455 mole) was then added dropwise over eight minutes. During the addition period, a slight exotherm was noticed and the flask was immersed in an ice bath to maintain the reaction temperature at 21.5° C. to 25.5° C. for 2.1 hours. The reaction mixture was permitted to settle overnight. The acid layer was removed, washed once with 30 mL EDC, and discarded. The combined EDC solutions were quenched with 2% NaHCO3 (600 mL), washed with deionized water (400 mL), 1% NaHCO3 solution (400 mL), deionized water (400 mL, twice), and stripped in vacuo. The resulting light yellow liquid weighed 48.9 g (89.5% yield), and contained 1.8% EDC and 98.2% dl- and meso-(4,5-dichloromethyl)-1,3-dioxolane, as determined by GC analysis and proton NMR (CDCl3) δ (s, --OCH2O--), 4.1 (m, ClCH2CHCHCH2Cl), 3.6(d, ClCH2CHCHCH2Cl).

Fuente