Reaktion #543537

ord-3eb9aa6ce62546f78904c2eb2703b578

Reaktionsgleichung

O=c1[nH]c(=O)c2cc(Cl)ccc2o1
6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione
CN(C)C=O
DMF
BrCCCCCCCCCCBr
1,10-dibromodecane
CN(C)C=O
DMF
CCN(C(C)C)C(C)C
Diisopropylethylamine
O=c1oc2ccc(Cl)cc2c(=O)n1CCCCCCCCCCBr
6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione
Ausbeute 49.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    Sonstigethe flask was placed in an oil bath
  3. 3
    TemperaturThe reaction was heated to 60 C
  4. 4
    Temperaturcooled to 47 C
  5. 5
    SonstigeThe resulting solids were removed by filtration
  6. 6
    WaschenThe aqueous layer was washed with warm hexanes
  7. 7
    FiltrationThe resulting solids were filtered from the hexane layer
  8. 8
    Sonstigerecrystallized
  9. 9
    Temperaturfrom warm hexanes

Vorschrift

A slurry of 9.77 g of 6-chloro-2H-1,3-benzoxazine-2,4(3H)-dione (50 mmol) and 60 ml of DMF was treated with a solution of 1,10-dibromodecane (52.52 g, 0.175 mol) and DMF (60 ml) was added. Diisopropylethylamine (9.6 ml, 55 mmol) was added dropwise. A thermometer and condenser were attached, and the flask was placed in an oil bath. The reaction was heated to 60 C. for approximately 3 hrs, cooled to 47 C. and hexanes (150 ml) were added. The mixture was diluted with water (175 ml). The resulting solids were removed by filtration. The aqueous layer was washed with warm hexanes. The resulting solids were filtered from the hexane layer and recrystallized from warm hexanes to give 10.39 g of 6-chloro-3-(10-bromodecyl)-2H-1,3-benzoxazine-2,4(3H)-dione.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07186414B2uspto-grants-2007_03