Reaktion #7433

ord-f9a41ba85d96457aa547e1997e89c67d

Reaktionsgleichung

N#N
N2
C=C(C)C(=O)O
Methacrylic acid
CC(C)(C)OC(=O)CBr
t-butyl bromoacetate
C1CCC2=NCCCN2CC1
DBU
C=C(C)C(=O)OCC(=O)OC(C)(C)C
t-butyl-2-methacryloyloxyacetate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeequipped with condenser, nitrogen inlet
  2. 2
    TemperaturThe mixture was cooled to room temperature
  3. 3
    Sonstigethe salt was removed by filtration
  4. 4
    WaschenThe toluene solution was washed with 75 ml saturated NaCl solution and 2×75 ml Dl-water respectively
  5. 5
    Sonstigebefore dried on MgSO4 overnight
  6. 6
    FiltrationThe solid was filtered out
  7. 7
    Sonstigethe toluene was removed at rotavap
  8. 8
    workup.DISTILLATIONAn oily residue was distilled to a final clear liquid at reduced pressure

Vorschrift

Methacrylic acid (8.06 g, 0.10 mole), t-butyl bromoacetate (19.50 g, 0.10 mole) and 1,8-diazabicyclo[5.4.0]undoc-7-ene, DBU, (15.20 g, 0.10 mole) and 150 ml toluene were combined in a 500 ml 3-neck flask equipped with condenser, nitrogen inlet, thermometer and magnetic stirrer bar. The reaction mixture was stirred at room temperature for one hour. The reaction was continued at 90° C. overnight under a blanket of N2 flow. The mixture was cooled to room temperature and the salt was removed by filtration. The toluene solution was washed with 75 ml saturated NaCl solution and 2×75 ml Dl-water respectively before dried on MgSO4 overnight. The solid was filtered out and the toluene was removed at rotavap. An oily residue was distilled to a final clear liquid at reduced pressure.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087356B2uspto-grants-2006_08