反応式
[Cl-].[Al+3].[Cl-].[Cl-].Cl.Cl[CH2:7][C:8]([NH:10][C:11]1[CH:16]=[CH:15][C:14]([F:17])=[C:13]([Cl:18])[CH:12]=1)=[O:9]>>[Cl:18][C:13]1[CH:12]=[C:11]2[C:16]([CH2:7][C:8](=[O:9])[NH:10]2)=[CH:15][C:14]=1[F:17]参加物
実験手順
A 26.63 g. sample of the N-(2-chloro)-2-chloro-4-fluoroaniline was thoroughly mixed with 64 g. of anhydrous aluminum chloride, and the mixture was heated at 210°-230° C. for 8.5 hours. The reaction mixture was then poured onto a mixture of ice an 1N hydrochloric acid, with stirring. Stirring was continued for 30 minutes, and then the solid was collected by filtration (22.0 g.). The solid was dissolved in 1:1 ethyl acetate-hexane and chromatographed on 800 g. of silica gel. Elution of the column, followed by evaporation of the fractions, produced 11.7 g. of the N-(2-chloroacetyl)-3-chloro-4-fluoroaniline, followed by 3.0 g. of 6-chloro-5-fluorine-2-oxindole. The latter material was recrystallized from toluene to give 1.70 g. (7% yield) of the title compound, m.p. 196°-206° C. Analysis by NMR spectroscopy indicated that the product was contaminated by some 4-chloro-5-fluorooxindole. A second crop weighing 0.8 g. was obtained.
後処理
- stirringStirring
- filtrationthe solid was collected by filtration (22.0 g.)
- dissolutionThe solid was dissolved in 1:1 ethyl acetate-hexane
- customchromatographed on 800 g
- washElution of the column
- customfollowed by evaporation of the fractions
- customproduced 11.7 g
- customThe latter material was recrystallized from toluene
- customto give 1.70 g
出典と根拠
- ORDレコード
- ord-648f109ece9742c68f0c921925e57cde
- 出典データセット
- uspto-grants-1988_02
- 特許番号
- US04725616
関連ノート
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