Réaction #2348105

Équation de réaction

Phosgene

1-(4,5-methylenedioxy-2-nitrophenyl)ethanol

Et2O hexane

→

solid

Rendement 85.0%

1-(4,5- methylenedioxy-2-nitrophenyl)ethyl chloroformate

Rendement 85.0%

Solvants

THF

Conditions de réaction

Traitement

1. 1
   AutreThe mixture was evaporated (an oil-less pump with downstream aqueous NaOH trap
2. 2
   Autreto remove the excess phosgene)
3. 3
   Autreto afford a viscous brown oil
4. 4
   AutrePurification
5. 5
   Lavageeluted with 20% Et2O/hexane

Mode opératoire

Phosgene (500 mL of 20% w/v in toluene from Fluka: 965 mmole; 4 eq.) was added slowly to a cold, stirring solution of 50 g (237 mmole; 1 eq.) of 1-(4,5-methylenedioxy-2-nitrophenyl)ethanol in 400 mL dry THF. The solution was stirred overnight at ambient temperature at which point TLC.(20% Et2O/hexane) indicated >95% conversion. The mixture was evaporated (an oil-less pump with downstream aqueous NaOH trap is recommended to remove the excess phosgene) to afford a viscous brown oil. Purification was effected by flash chromatography on a short (9×13 cm) column of silica gel eluted with 20% Et2O/hexane. Typically 55 g (85%) of the solid yellow MeNPOC-Cl is obtained by this procedure. The crude material has also been recrystallized in 2-3 crops from 1:1′ether/hexane. On this scale, ˜100 ml is used for the first crop, with a few percent THF added to aid dissolution, and then cooling overnight at −20° C. (this procedure has not been optimized). The product should be stored desiccated at −20° C.

Source