反応 #65401

ord-501f70b46e3f4601b7c88282c61ae676

反応方程式

CC1(C)Oc2ccc([N+](=O)[O-])cc2NC1=O
3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-2H-1,4-benzoxazine
[H-].[Na+]
sodium hydride
O=C(CBr)c1ccccc1
phenacyl bromide
CC1(C)Oc2ccc([N+](=O)[O-])cc2N(CC(=O)c2ccccc2)C1=O
3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazine
収率 66.6%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe mixture was stirred at room temperature for 1 hour
  2. 2
    workup.DISTILLATIONafter which the solvent was distilled off under reduced pressure
  3. 3
    workup.ADDITIONThe residue was diluted with 50 ml of water
  4. 4
    抽出extracted with ethyl acetate
  5. 5
    乾燥The extract was dried over anhydrous magnesium sulfate
  6. 6
    濃縮concentrated under reduced pressure
  7. 7
    その他The residue was chromatographed on a silica gel column and elution
  8. 8
    その他Recrystallization from ethyl acetate-ether

実験手順

In an argon gas stream, 2.0 g of 3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-2H-1,4-benzoxazine was added gradually to 0.4 g of 60% sodium hydride in oil in 40 ml of dry N,N-dimethylformamide. The mixture was stirred at room temperature for 1 hour and 2.68 g of phenacyl bromide was added. The mixture was stirred at room temperature for 1 hour, after which the solvent was distilled off under reduced pressure. The residue was diluted with 50 ml of water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was chromatographed on a silica gel column and elution was carried out with methylene chloride-ethyl acetate. Recrystallization from ethyl acetate-ether gave 2.04 g of 3,4-dihydro-2,2-dimethyl-6-nitro-3-oxo-4-phenacyl-2H-1,4-benzoxazine.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05420126uspto-grants-1995_05