Acetone → [Bis(4-dimethylaminophenyl)(2-methylindol-3-yl)]methane

HRID 637863

反応式

HRID 637863 の反応式
[OH-].[K+].[CH3:3][N:4]([CH3:31])[C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:12]([C:22]3[CH:27]=[CH:26][C:25]([N:28]([CH3:30])[CH3:29])=[CH:24][CH:23]=3)=[C:13](S(C)(=O)=O)[CH:14]=[CH:15][C:16]=2[CH3:17])=[CH:7][CH:6]=1.[CH3:32][C:33]1[NH:34]C2C(C=1)=CC=CC=2.[CH3:42]C(C)=O>O.C(O)(C)C>[CH3:29][N:28]([CH3:30])[C:25]1[CH:26]=[CH:27][C:22]([C:12]2[C:11]([C:8]3[CH:9]=[CH:10][C:5]([N:4]([CH3:3])[CH3:31])=[CH:6][CH:7]=3)=[C:16]3[C:15](=[CH:14][CH:13]=2)[NH:34][C:33]([CH3:32])=[C:17]3[CH3:42])=[CH:23][CH:24]=1

参加物

7

反応物 4

HCID 180AcetoneHCID 72242-MethylindoleHCID 14797Potassium HydroxideHCID 20184810[Bis(4-dimethylaminophenyl)(4-methylphenylsulfonyl)]methane

生成物 1

HCID 20184812[Bis(4-dimethylaminophenyl)(2-methylindol-3-yl)]methane

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 3776Isopropanol溶媒

実験手順

Two grams of potassium hydroxide was added slowly to a mixture of 6.3 g of [bis(4-dimethylaminophenyl)(4-methylphenylsulfonyl)]methane, 2.5 g of 2-methylindole and 75.0 ml of acetone. The resulting slurry was stirred for approximately 24 hours at ambient temperature. Fifty milliliters of isopropyl alcohol was added to the reaction mixture to effect complete solution. Slowly with stirring, the resulting solution was added to one liter of water and the solid which formed was collected by filtration. The wet filter cake was suspended in 100.0 ml of isopropyl alcohol and stirred approximately thirty minutes. The solid was collected by filtration, washed twice with 25.0 ml of isopropyl alcohol each and dried to obtain 5.1 g of [bis(4-dimethylaminophenyl)(2-methylindol-3-yl)]methane (Formula IV: R1 =R2 =R4 =R9 =R11 =H; R3 =R5 =N(CH3)2 ; R10 =CH3), a pale gray-colored solid which melted at 198°-202° C. A significant infrared maximum appeared at 740 (C--H;s) cm-1. The nuclear magnetic resonance spectrum was concordant with the assigned structure. A toluene solution of the product spotted on an acid clay-coated paper or a phenolic resin-coated paper slowly developed a grape-colored image.

後処理

  1. stirringSlowly with stirring
  2. customthe solid which formed
  3. filtrationwas collected by filtration
  4. stirringstirred approximately thirty minutes
  5. filtrationThe solid was collected by filtration
  6. washwashed twice with 25.0 ml of isopropyl alcohol each and
  7. customdried

出典と根拠

ORDレコード
ord-972f759569bd4d7381a40d3ab6b88287
出典データセット
uspto-grants-1985_12
特許番号
US04558137

関連ノート

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