反应 #543537

ord-3eb9aa6ce62546f78904c2eb2703b578

反应方程式

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
收率 49.9%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    其他the flask was placed in an oil bath
  3. 3
    温度The reaction was heated to 60 C
  4. 4
    温度cooled to 47 C
  5. 5
    其他The resulting solids were removed by filtration
  6. 6
    洗涤The aqueous layer was washed with warm hexanes
  7. 7
    过滤The resulting solids were filtered from the hexane layer
  8. 8
    其他recrystallized
  9. 9
    温度from warm hexanes

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186414B2uspto-grants-2007_03