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HRID 1274523생성일: 2026년 10월 26일

Chloroacetyl chloride → 6-Di-n-butylamino-2-(6-di-n-butylamino-3-oxo-2(3H)-benzofuranylidene)-3(2H)-benzofuranone

https://huagongshe.com/reaction/1274523

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물N,N-Dibutyl-3-aminophenolHCID 601234—
용매ChloroformHCID 6212—
생성물6-Di-n-butylamino-2-(6-di-n-butylamino-3-oxo-2(3H)-benzofuranylidene)-3(2H)-benzofuranoneHCID 54492553—

반응 단계

1.8 g (8.1 mmol) of 3-di-n-butylamino-phenol are dissolved in 20 ml of dry chloroform with exclusion of moisture. 0.7 ml (8.8 mmol) of chloroacetyl chloride is added dropwise with vigorous stirring. Silica gel (about 10 g in total) is then allowed to trickle in until a large proportion of the reaction solution has been absorbed, and the mixture is boiled under reflux for 15 hours. Finally, the solid is filtered off and washed with chloroform until the wash solution remains virtually colourless. The organic phases are combined. After the solvent has been stripped off on a rotary evaporator, 1.4 g of a dark brown, highly viscous crude product are obtained. Working up of the crude product by column chromatography over silica gel using chloroform as the solvent gives the oxindigo colorant as a red-violet fraction in the first runnings. After the chloroform has been stripped off, the resulting colorant is dried under an oil pump vacuum at 75° C. for 5 hours.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06156914
출처 데이터셋uspto-grants-2000_12
ORD IDord-387728e2f1d4409fa27033da663818c9
출처 메모uspto-grants-2000_12