Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2323Erstellt: 24. Oktober 2026

Acetone → 4,4'-Diamino-6-cyanobenzanilide

https://huagongshe.com/de/reaction/2323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktAmmonium HydroxideHCID 14923—
EduktFuming sulfuric acidHCID 24681—
Edukt4,4'-Diamino-6-carbamoyl benzanilideHCID 19689751—
LösungsmittelEthanolHCID 702—
Produkt4,4'-Diamino-6-cyanobenzanilideHCID 19689750—

Reaktionsschritte

350 ml of oleum (30% by weight) was cooled down below 0° C. using an ice bath, 99.6 g (0.368 mol) of 4,4'-diamino-6-carbamoyl benzanilide in a powder form was added below 5° C. with stirring. The stirring was continued to the next day, and the solution was neutralized by adding 1100 ml of NH4OH (28% by weight) already cooled down to -5° to 0° C. The solution was sufficiently washed to remove salt by filtering and washed with a small amount of warm ethanol and then dried in a vacuum oven at 80° C. The dried reactant which was mixed with by-products was extracted by soxlet and treated with the activated carbon and then ethanol was added to recrystallize in the mixture solvent (acetone:ethanol=1:1). The light yellow-scalelike crystal was filtered and dried in a vacuum oven at 80° C. The light yellow-scalelike crystal was extracted again by soxlet with acetone and treated with the activated carbon. And then the white-scalelike crystal obtained by recrystalling in the mixture solvent (acetone:ethanol=1:1) was dried in a vacuum oven at 80° C. (40 g of the raw material was obtained and the boiling point thereof was 250° to 251° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728799
Quelldatensatzuspto-grants-1998_03
ORD IDord-202ad24f23144e29a486e05cf3ccb4db
Quellennotizuspto-grants-1998_03