Methanol → N-[3-(1,3-dioxolyl)phenyl]isatin

HRID 1431911

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HRID 1431911 반응식
[NH:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[C:2]1=[O:3].[H-].[Na+].Br[C:15]1[CH:16]=[C:17]([CH:21]2[O:25][CH2:24][CH2:23][O:22]2)[CH:18]=[CH:19][CH:20]=1.CO>CN(C=O)C.C(Cl)(Cl)Cl.[Cu]I>[O:22]1[CH:23]=[CH:24][O:25][CH:21]1[C:17]1[CH:16]=[C:15]([N:1]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:4](=[O:5])[C:2]2=[O:3])[CH:20]=[CH:19][CH:18]=1

참가 물질

8

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온도
0 °C

실험 절차

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.

후처리

  1. temperaturecooled in an ice bath under a nitrogen atmosphere
  2. temperatureThe resulting suspension was heated in an oil-bath under nitrogen at 130-140° C. for 16 hours
  3. temperatureIt was then cooled to room temperature
  4. filtrationThis suspension was filtered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customA viscous brown oil was recovered which
  7. customwand evaporated to dryness
  8. customsuch for the next reaction

출처 및 근거

ORD 기록
ord-a832cacbd4894615a14088b86f00fefb
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07611909B1

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