Reacción #2467926

ord-89c519da4006402697625f65f8045746

Ecuación de reacción

C(=NC1CCCCC1)=NC1CCCCC1
Dicyclohexylcarbodiimide
O=C(O)CC(=O)O
Malonic acid
CC(O)c1ccccc1
1-phenyl-ethanol
O=C(NC1CCCCC1)NC1CCCCC1
dicyclohexyl urea

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawith cooling over 10 min so the temperature
  2. 2
    Otrodid not exceed 30° C

Procedimiento

Malonic acid (12 g, 0.11 mol) was dissolved in acetonitrile (450 mL) in an Erlenmeyer flask (1 L) together with 1-phenyl-ethanol (26 g, 0.22 mol). Dicyclohexylcarbodiimide (45 g) was added in portions and with cooling over 10 min so the temperature did not exceed 30° C. A precipitate of dicyclohexyl urea formed almost immediately. Stirring at RT continued over the week-end to complete the reaction. Dicyclohexyl urea was removed by filtration and the filter cake was washed with addition acetonitrile (10 mL). The combined solution was evaporated in vacuum to give the crude product as colourless oil. Yield: 29 g, 93%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08257786B2uspto-grants-2012_09