Reaction #465934

ord-745b32d32d88497f9e058ee30296b5c4

Reaction equation

O=Cc1ccc(Cl)cc1
p-chlorobenzaldehyde
C1COCCN1
morpholine
O
water
Clc1ccc(C(N2CCOCC2)N2CCOCC2)cc1
product
Clc1ccc(C(N2CCOCC2)N2CCOCC2)cc1
1-Chloro-4-(dimorpholinomethyl)-benzene

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherOver the course of 45 minutes, 8.4 ml of water were removed azeotropically
  2. 2
    workup.WAITThe mixture was left
  3. 3
    Temperatureto cool with slow stirring
  4. 4
    OtherAt 58° C.
  5. 5
    Othervery fine crystals slowly precipitated out
  6. 6
    TemperatureThe mixture was cooled in an ice bath to +5° C
  7. 7
    OtherAfter a post-stirring time of 1 hour, the solid which had precipitated out
  8. 8
    Filtrationwas filtered off with suction
  9. 9
    WashThe white product was washed with 2×50 ml of methylcyclohexane
  10. 10
    Otherdried overnight in a drying cabinet at 20° C.

Procedure

70 g of p-chlorobenzaldehyde and 105 g of morpholine were heated to boiling in 260 g of methylcyclohexane in a water separator. Over the course of 45 minutes, 8.4 ml of water were removed azeotropically. The mixture was left to cool with slow stirring. At 58° C., the solution was seeded, and very fine crystals slowly precipitated out. The mixture was cooled in an ice bath to +5° C. After a post-stirring time of 1 hour, the solid which had precipitated out was filtered off with suction. The white product was washed with 2×50 ml of methylcyclohexane and dried overnight in a drying cabinet at 20° C. and 100 mbar. 129.2 g of product were obtained in the form of white crystals (87% of theory).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06296788B1uspto-grants-2001_10