Reacción #2304285

ord-6534ea555fb44d4b8ef0b9cb12415823

Ecuación de reacción

NC[C@H]1CC[C@H](C(=O)O)CC1
trans-4-(aminomethyl)cyclohexanecarboxylic acid
O=C(Cl)OCc1ccccc1
benzyl chloroformate
O=C(NCC1CCC(C(=O)O)CC1)OCc1ccccc1
23
Rendimiento 96.1%
O=C(NCC1CCC(C(=O)O)CC1)OCc1ccccc1
4-{[(phenylmethoxy)carbonylamino]methyl}cyclohexanecarboxylic acid
Rendimiento 96.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction temperature was maintained below 10° C
  2. 2
    LavadoThe clear solution was washed with ether (3×80 ml)
  3. 3
    workup.ADDITIONby adding 6N HCl
  4. 4
    FiltraciónThe precipitates were filtered
  5. 5
    Otrodried in vacuo

Procedimiento

To a solution of trans-4-(aminomethyl)cyclohexanecarboxylic acid (10 g, 63.6 mmol, Aldrich) in 2N aqueous NaOH (65 ml) at 0° C. was added benzyl chloroformate (11.9 g, 70 mmol, Aldrich) and the reaction temperature was maintained below 10° C. The cloudy mixture was stirred at RT for 0.5 h. It was then diluted with H2O (100 ml). The clear solution was washed with ether (3×80 ml). The pH of the aqueous layer was adjusted to 2 by adding 6N HCl. The precipitates were filtered and dried in vacuo. 17.8 g of 23 was obtained as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07407644B2uspto-grants-2008_08