Reacción #64244
ord-e1b24c9a3ef84fc4ae523d33295482bf
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturais heated for 2 h to 60° C.
- 2workup.ADDITIONmixed
- 3OtroOne leaves
- 4SecadoAfter neutralisation with saturated sodium hydrogen carbonate solution, the organic phase is dried with sodium sulphate
- 5workup.DISTILLATIONdistilled off in a vacuum
- 6FiltraciónAfter trituration with ether, the crystals are filtered off with suction
Procedimiento
A mixture of 6.8 ml (0.072 mol) acetic acid anhydride and 2.8 ml (0.072 mol) formic acid is heated for 2 h to 60° C. and thereafter mixed, with cooling at 5° C., with 1.9 g (0.012 mol) trans-4-nitroxycyclohexylamine. One leaves to stir overnight at room temperature, subsequently dilutes with 100 ml ethyl acetate and adds 100 ml of water thereto. After neutralisation with saturated sodium hydrogen carbonate solution, the organic phase is dried with sodium sulphate and distilled off in a vacuum. After trituration with ether, the crystals are filtered off with suction. One obtains 1.5 g of the title compound of the m p 148°-150° C., i.e. 66% of theory.