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HRID 637863作成日:2026年10月25日

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

https://huagongshe.com/reaction/637863

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物2-MethylindoleHCID 7224—
反応物Potassium HydroxideHCID 14797—
反応物[Bis(4-dimethylaminophenyl)(4-methylphenylsulfonyl)]methaneHCID 20184810—
溶媒WaterHCID 962—
溶媒IsopropanolHCID 3776—
生成物[Bis(4-dimethylaminophenyl)(2-methylindol-3-yl)]methaneHCID 20184812—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04558137
出典データセットuspto-grants-1985_12
ORD IDord-972f759569bd4d7381a40d3ab6b88287
出典メモuspto-grants-1985_12