反応 #1519093

ord-a832cacbd4894615a14088b86f00fefb

反応方程式

Brc1cccc(C2OCCO2)c1
2-(3-bromophenyl)-1,3-dioxolane
CO
methanol
[H-].[Na+]
sodium hydride
O=C1Nc2ccccc2C1=O
Isatin
O=C1C(=O)N(c2cccc(C3OC=CO3)c2)c2ccccc21
N-[3-(1,3-dioxolyl)phenyl]isatin

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled in an ice bath under a nitrogen atmosphere
  2. 2
    温度The resulting suspension was heated in an oil-bath under nitrogen at 130-140° C. for 16 hours
  3. 3
    温度It was then cooled to room temperature
  4. 4
    ろ過This suspension was filtered
  5. 5
    濃縮the filtrate was concentrated under reduced pressure
  6. 6
    その他A viscous brown oil was recovered which
  7. 7
    その他wand evaporated to dryness
  8. 8
    その他such for the next reaction

実験手順

Isatin (3.2 g, 0.0218 moles) was dissolved in anhydrous DMF (75 mL) and cooled in an ice bath under a nitrogen atmosphere. To this cold solution, sodium hydride (0.575 g, 0.0239 moles) was added and the reaction was stirred at 0° C. for 1.5 hours. This solution was then treated with 2-(3-bromophenyl)-1,3-dioxolane (5 g, 1 equivalent) followed by CuI (8.3 g, 2 equivalents). The resulting suspension was heated in an oil-bath under nitrogen at 130-140° C. for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. This suspension was filtered and the filtrate was concentrated under reduced pressure. A viscous brown oil was recovered which was suspended in a xylenes (150 mL) wand evaporated to dryness. The residue was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion; Rf (product)=0.86.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07611909B1uspto-grants-2009_11