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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1274523Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1274523

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
EduktN,N-Dibutyl-3-aminophenolHCID 601234—
LösungsmittelChloroformHCID 6212—
Produkt6-Di-n-butylamino-2-(6-di-n-butylamino-3-oxo-2(3H)-benzofuranylidene)-3(2H)-benzofuranoneHCID 54492553—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06156914
Quelldatensatzuspto-grants-2000_12
ORD IDord-387728e2f1d4409fa27033da663818c9
Quellennotizuspto-grants-2000_12