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

HRID 2373103

反応式

HRID 2373103 の反応式
[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

参加物

8

反応物 4

HCID 887MethanolHCID 7054IsatinHCID 24758Sodium hydrideHCID 873062-(3-Bromophenyl)-1,3-dioxolane

生成物 1

HCID 21972258N-[3-(1,3-dioxolyl)phenyl]isatin

試薬・触媒・溶媒 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 6212Chloroform溶媒2 回HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

Isatin (3.2 g, 0.0218 mol) 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 mol) 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 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.

後処理

  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

出典と根拠

ORDレコード
ord-78d644b5ac7f45c9abd6540cce382ef6
出典データセット
uspto-grants-2008_12
特許番号
US07459284B2

関連ノート

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