Reaktion #94370

Reaktionsgleichung

1-chloro-2-pyrrolidino ethane

4-adamantyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline dihydrochloride dihydrate

N-Methyl-p-(1-adamantyloxy)aniline

→

4-Adamantoyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline Dihydrochloride Dihydrate

Lösungsmittel

toluene

pentane

C6H6

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturat reflux for 18 hours
2. 2
   Temperaturto cool
3. 3
   Waschenwashed with H2O and brine
4. 4
   workup.DISSOLUTIONwas dissolved in CH2Cl2
5. 5
   workup.ADDITIONtreated with 10 ml
6. 6
   Sonstigewas recrystallized from CH2Cl2
7. 7
   SonstigeCH3CN to yield 1.93 g

Vorschrift

To an ice-MeOH cooled solution of 2.0 g. (0.0078 mole) of N-Methyl-p-(1-adamantyloxy)aniline in 20 ml. THF was added 4.75 ml. of 1.64 N Buli in pentane. A solution of a 1:1 mixture of toluene, and 1-chloro-2-pyrrolidino ethane (2.08 g.) in 20 ml. THF was then added and the mixture stirred at room temperature for 1 hour and at reflux for 18 hours. The solution was allowed to cool, diluted with C6H6 and washed with H2O and brine. The residue remaining when the organic fraction was taken to dryness was dissolved in CH2Cl2, treated with 10 ml. HCl saturated Et2O and taken to dryness The residual solid was recrystallized from CH2Cl2 :CH3CN to yield 1.93 g. (55%) of 4-adamantyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline dihydrochloride dihydrate, m.p. 189°-190° (efervess).

Quelle