Reaktion #96020

ord-5b4af2fb8ab446f3ba9604998ad8040e

Reaktionsgleichung

Br.CC(=O)CC(=O)N1CCNCC1
1-acetoacetylpiperazine hydrobromide
CCN(CC)CC
Triethylamine
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)N1CCN(C(=O)CC(C)=O)CC1
4-acetoacetyl-1-methacryloylpiperazine
Ausbeute 56.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction solution was filtered
  2. 2
    Sonstigethe solvent was removed at low vacuum
  3. 3
    workup.DISTILLATIONThe residue was distilled

Vorschrift

Crude 1-acetoacetylpiperazine hydrobromide (50 g, 0.2 mole) was dissolved in N,N-dimethylformamide (300 ml) with AranoxTM (50 mg) (available from U.S. Rubber Co.). Triethylamine (50 g, 0.5 mole) was added at 0° C., followed immediately by the dropwise addition of methacryloyl chloride (20.8 g, 0.2 mole) at 0° C. The reaction solution was then allowed to reach 20° C. over a 20 hour period. The reaction solution was filtered and the solvent was removed at low vacuum. The residue was distilled to give 4-acetoacetyl-1-methacryloylpiperazine (b.p.=110°-129° C./10-8μ) at a yield of 56%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04346231uspto-grants-1982_08