Reaction #1994244

ord-ebbeb5a3f0654a4391d3adacf6daeca0

Reaction equation

NC(CCCC(=O)O)C(=O)O
racemic 2-aminoadipic acid
CC(=O)OC(C)=O
acetic anhydride
CCN(CC)CC
triethylamine
CC(=O)C1CCCC(=O)N1C(C)=O
N,6-diacetyl-piperidin-2-one

Conditions

Temperature
60°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe crude reaction product
  2. 2
    Concentrationis concentrated as
  3. 3
    Othermuch as possible (rotary evaporator and vane pump)
  4. 4
    Washwashed with water (5×20 mL)
  5. 5
    ExtractionThe water washings are extracted with CH2Cl2 (2×20 mL)
  6. 6
    Concentrationconcentrated
  7. 7
    OtherPurification of 8
  8. 8
    OtherThe fractions are dried
  9. 9
    Concentrationconcentrated
  10. 10
    Otherthe product crystallized in the form of pale yellow flakes

Procedure

A 50-mL round bottom flask is charged with racemic 2-aminoadipic acid (2.3 g, 1.43×10−3 mol) and triethylamine (7.5 mL), acetic anhydride (7.5 mL), and a catalytic amount of DMAP (15 mg). The mixture is heated to 60° C. for 24 h; the progress of the reaction is followed by TLC (eluent: ethyl acetate/petroleum ether, 8/2). Once the reaction is complete, the crude reaction product is concentrated as much as possible (rotary evaporator and vane pump) and then washed with water (5×20 mL). The water washings are extracted with CH2Cl2 (2×20 mL). The organic layers are combined and concentrated. Purification of 8 is carried out on a silica gel column (eluent: ethyl acetate/petroleum ether, 8/2). The fractions are dried, concentrated and the product crystallized in the form of pale yellow flakes.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08597706B2uspto-grants-2013_12