Abstract:
A PROCESS FOR THE PREPARATION OF FAST DYEINGS AND PRINTS ON FIBROUS MATERIALS CONTAINING HYDROXY GROUPS OR NITROGEN, WHICH PROCESS COMPRISES APPLYING WATER-SOLUBLE ORGANIC DYESTUFFS WHICH CONTAIN AT LEAST A GROUP OF THE FORMULA
-SO2-CH2-CH2-O-CO-NH-X
IN THE MOLECULE IN WHICH GROUP X IS A HYDROGEN ATOM OR AN -SO3H- GROUP ON THE SAID FIBROUS MATERIALS AND FIXING THEM AT NORMAL OR AT ELEVATED TEMPERATURE OR UNDER THE ACTION OF HEAT YIELDING VERY VALUABLE, INTENSE DYEINGS AND PRINTS WICH ARE VERY STABLE WHEN BEING SUBJECTED TO TREATMENTS OF WASHING AND TO THE ACTION OF LIGHT. THEY HAVE ALSO A REMARKABLE FASTNESS TO WATER, SEAWATER, RUBBING, IRONING, ACIDS, ALKALIS AND SOLVENTS. WHEN BEING FINISHED AFTERWARDS WITH SYNTHETIC RESINS IN AN ACID MEDIUM, DYEINGS AND PRINTS OF THE INVENTION SHOW ADVANTAGEOUS PROPERTIES.
Abstract:
N-acetoacetyl-2,5-dimethoxy-4-chloroanilide is obtained in high yield and purity by suspending 2,5-dimethoxy-4-chloroaniline in water and adding the complete amount of diketene necessary altogether at the beginning of the reaction. The product is obtained in a purity allowing its use as an azoic coupling component without purification.
Abstract:
5-Acetoacetylamino benzimidazolone-(2) is obtained in high yield and excellent purity by reacting diketene with the aqueous solution of a salt of 5-amino-benzimidazolone-(2) and an acid having a pKa value of 1 to 7, preferably in the presence of an antioxidant and/or a reducing agent.
Abstract:
1527892 Preparation of 4-chloro-2,5-dimethoxyaniline HOECHST AG 25 Nov 1975 [25 Nov 1974] 48445/75 Heading C2C 4 - Chloro - 2,5 - dimethoxyaniline or a salt thereof is obtained by treating a mixture comprising water and particles of 4-chloro-2,5- dimethoxynitrobenzene having an average size of less than 100 microns with hydrogen in the presence of a nickel catalyst, and if desired, converting the 4-chloro-2,5-dimethoxyaniline to a salt thereof.
Abstract:
N-acetoacetyl-2,5-dimethoxy-4-chloroanilide is obtained in high yield and purity by suspending 2,5-dimethoxy-4-chloroaniline in water and adding the complete amount of diketene necessary altogether at the beginning of the reaction. The product is obtained in a purity allowing its use as an azoic coupling component without purification.