GB425517A - Manufacture of dyestuffs - Google Patents
Manufacture of dyestuffsInfo
- Publication number
- GB425517A GB425517A GB1990434A GB1990434A GB425517A GB 425517 A GB425517 A GB 425517A GB 1990434 A GB1990434 A GB 1990434A GB 1990434 A GB1990434 A GB 1990434A GB 425517 A GB425517 A GB 425517A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxy
- group
- condensing
- leuco
- anthraquinone
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/325—Dyes with no other substituents than the amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Anthraquinone dyes of the formula <FORM:0425517/IV/1> wherein x stands for an oxyalkyl residue and y for a residue of the benzene series containing an NH2-group or an OH-group in p-position to the amino group (the groups NHx and NHy being the sole nuclear substituents in the anthraquinone nucleus), by condensing a leucobody of a 1-oxy-4-(4<1>-amino- or 4<1>-oxy)-phenylaminoanthraquinone with an oxyalkylamine; or by condensing a leuco body of a 1-oxy-4-oxyalkylaminoanthraquinone with a primary amine of the benzene series containing in p-position to the amino group a further NH2-group or an - OH group, and in either case oxidizing the condensation product to the anthraquinone derivative during or after the condensation. In an example, leuco-1-oxy-4-(4<1>-aminophenyl)-aminoanthraquinone is condensed with b -oxyethylamine in presence of sodium chlorate and boric acid in alcohol (acetate artificial silk is dyed green shades). A sample furnished under Sect. 2 (5) is prepared by condensing leuco-1-oxy-4-b -oxyethylaminoanthraquinone with p-aminophenol in presence of sodium chlorate and boric acid in methyl alcohol (blue-green shades on acetate artificial silk). Specification 423,256 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1990434A GB425517A (en) | 1933-09-20 | 1933-09-20 | Manufacture of dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1990434A GB425517A (en) | 1933-09-20 | 1933-09-20 | Manufacture of dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB425517A true GB425517A (en) | 1935-03-15 |
Family
ID=10137076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1990434A Expired GB425517A (en) | 1933-09-20 | 1933-09-20 | Manufacture of dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB425517A (en) |
-
1933
- 1933-09-20 GB GB1990434A patent/GB425517A/en not_active Expired
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