Reacción #362397

Ecuación de reacción

1-acetoxy-4-dibenzylamino-2-butene

dicyclohexylmethylamine

→

title compound

N,N-Dicyclohexylmethyl-N',N'-dibenzyl-2-butene-1,4-diamine

Disolventes

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   ConcentraciónThe reaction mixture is concentrated in vacuo to a solid which
2. 2
   workup.DISSOLUTIONis redissolved in 100 ml of THF
3. 3
   workup.ADDITIONtreated with 25 ml of 20% aqueous sodium hydroxide
4. 4
   workup.STIRRINGThe mixture is stirred for one hour
5. 5
   Concentraciónconcentrated
6. 6
   Extracciónextracted with diethyl ether
7. 7
   SecadoThe ether extracts are dried
8. 8
   Concentraciónconcentrated
9. 9
   Otroto give a solid which
10. 10
    Otrois then purified by crystallization from isopropanol

Procedimiento

A solution of 1-acetoxy-4-dibenzylamino-2-butene (10.1 g, 33 mmol) and dicyclohexylmethylamine (6.8 g, 32 mmol) in 50 ml of THF is treated with tetrakis(triphenylphosphine)palladium(0) (1.0 g, 0.9 mmol) and stirred at room temperature overnight. The reaction mixture is concentrated in vacuo to a solid which is redissolved in 100 ml of THF and treated with 25 ml of 20% aqueous sodium hydroxide. The mixture is stirred for one hour, concentrated and extracted with diethyl ether. The ether extracts are dried and concentrated to give a solid which is then purified by crystallization from isopropanol. The title compound is obtained in a yield of 9.7 g (65%) as a white solid melting at 61°-62° C.

Fuente