Reacción #65642

Ecuación de reacción

1-(2-Methoxyphenyl)piperazine

atropic acid

→

product

α-{1-[4-(2-Methoxyphenyl)piperazinyl]methyl}-benzeneacetic acid

Disolventes

ethanol

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaunder reflux for 18 hours
2. 2
   Otroevaporated in vacuo
3. 3
   OtroThe solid was triturated with acetone (3×100 ml)

Procedimiento

1-(2-Methoxyphenyl)piperazine (22.6 g; 0.118 mol) and atropic acid (174 g, 0.118 moll in ethanol (300 ml) were heated under reflux for 18 hours, cooled to room temperature, and evaporated in vacuo. The solid was triturated with acetone (3×100 ml) to give a first crop of product (13.8 g) as white crystals. The filtrate was evaporated in vacuo to give an oil which slowly crystallised over 1 month. The solid was triturated with acetone (200 ml) to give a second crop of the hemihydrate of the product (9.01 g) as white crystals, m.p. 160°-163°. (Found: C, 68.4; H, 7.2; N, 7.9. C20H24N2O3.0.5H2O requires C, 68.8; H, 7.2; N, 8.0%.)

Fuente