Reacción #456004

Ecuación de reacción

3-chlorophenethyl alcohol

3-chloropropionaldehyde diethyl acetal

→

6-chloro-1-(2-chloroethyl)isochroman

Disolventes

nitromethane

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturais cooled in an ice/water bath
2. 2
   Temperaturathe mixture is heated at 45° for 3 hr
3. 3
   TemperaturaAfter cooling
4. 4
   workup.ADDITIONthe mixture is poured onto ice/aqueous hydrochloric acid (1N)
5. 5
   Extracciónextracted with dichloromethane
6. 6
   Filtraciónfiltered through a pad of Celite
7. 7
   ConcentraciónThe filtrate is concentrated
8. 8
   Otrochromatographed twice on silica gel eluting with ethyl acetate/hexane (5/95)
9. 9
   Concentraciónconcentrated

Procedimiento

A mixture of 3-chlorophenethyl alcohol (XLV, 5.9055 g, 0.0398 mol), 3-chloropropionaldehyde diethyl acetal (LXII, 7.2 ml, 0.0430 mol) and nitromethane (3 ml) is cooled in an ice/water bath. Titanium tetrachloride (1M in dichloromethane, 88 ml, 0.088 mol) is added dropwise and the mixture is heated at 45° for 3 hr. After cooling, the mixture is poured onto ice/aqueous hydrochloric acid (1N) and extracted with dichloromethane. The combined organic layers are backwashed with hydrochloric acid (1N) and filtered through a pad of Celite topped with sodium sulfate. The filtrate is concentrated and chromatographed twice on silica gel eluting with ethyl acetate/hexane (5/95). The appropriate fractions are pooled and concentrated to give 6-chloro-1-(2-chloroethyl)isochroman (LXIV), NMR (CDCl3) 2.23, 2.70, 2.93, 3.75, 4.09, 4.89, 7.01 and 7.16 δ.

Fuente