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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1995247생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1995247

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물2-MethylindoleHCID 7224—
반응물Potassium HydroxideHCID 14797—
반응물[Bis(4-dimethylaminophenyl)(4-methylphenylsulfonyl)]methaneHCID 20184810—
용매WaterHCID 962—
용매IsopropanolHCID 3776—
생성물[Bis(4-dimethylaminophenyl)(2-methylindol-3-yl)]methaneHCID 20184812—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04403791
출처 데이터셋uspto-grants-1983_09
ORD IDord-01a1d9c2bc4a4f18956378bfa82b482e
출처 메모uspto-grants-1983_09