CH208544A - Process for the production of a nitrogen-containing condensation product. - Google Patents
Process for the production of a nitrogen-containing condensation product.Info
- Publication number
- CH208544A CH208544A CH208544DA CH208544A CH 208544 A CH208544 A CH 208544A CH 208544D A CH208544D A CH 208544DA CH 208544 A CH208544 A CH 208544A
- Authority
- CH
- Switzerland
- Prior art keywords
- nitrogen
- condensation product
- production
- containing condensation
- anthraquinone
- Prior art date
Links
- 239000007859 condensation product Substances 0.000 title claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000000034 method Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 claims description 4
- 240000007817 Olea europaea Species 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- 229920000742 Cotton Polymers 0.000 claims 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
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
- C09B1/48—Anthrimides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines stickstoffhaltigen Kondensationsproduktes. Es wurde gefunden, dass man ein stick stoffhaltiges Kondensationsprodukt herstellen kann, wenn man 1-Halogerr-2-methylanthr,a- chinon mit 1-Amirro-4-berrzoylanrinoarrtlrra- chinon umsetzt. Der neue Farbstoff ist ein violettblarres Pulver, das sich in Schwefel i -e mit olivgrüner Farbe löst und Baum s äLii wolle aus brauner Küpe in oliven Farbtönen färbt.
Als 1-Halogerr-2-methylarrthrachirronkann beispielsweise 1-Chlor-2-methylarrthrachirrorr verwendet werden.
Die Umsetzung mit 1-Amirro-4-benzoyl- amirroanthrachirron erfolgt zweckmässig in Gegenwart von LÖsnngs- oder Verteilungs mitteln, z. B. Nitrobenzol, Dichlorbenzol oder Naphthalin, und in Gegenwart von Kataly satoren, wie Kupfer oder Kupferverbindungen, sowie vorzugsweise in Anwesenheit von säure bindenden Mitteln, wie Natriumacetat und Alkalikarbonat, bei höherer Temperatur.
<I>Beispiel:</I> 25,6 Teile 1-Chlor-2-nrethylantbrachinon, 34,3 Teile 1.4-Monobenzoyldiämirroanthra- chirron, 20 Teile wasserfreies Natriumcarbo- nat, 1 Teil Kupferacetat und 350 Teile Nitro- benzol werden 3 Stunden zum Sieden erhitzt. Das Umsetzungsprodukt, das in Nadeln aus kristallisiert, wird kalt durch Filtration ab geschieden.
Process for the production of a nitrogen-containing condensation product. It has been found that a nitrogen-containing condensation product can be prepared if 1-halo-2-methylanthr, a-quinone is reacted with 1-amirro-4-berrzoylanrinoarrtlrra-quinone. The new dye is a violet-blue powder that dissolves in sulfur i -e with an olive-green color and dyes tree s äLii wool from a brown vat in olive hues.
As the 1-halo-2-methylarrthrachirron, for example 1-chloro-2-methylarrthrachirron can be used.
The reaction with 1-amirro-4-benzoyl amirroanthrachirron is expediently carried out in the presence of solvents or distribution agents, eg. B. nitrobenzene, dichlorobenzene or naphthalene, and in the presence of catalysts, such as copper or copper compounds, and preferably in the presence of acid-binding agents, such as sodium acetate and alkali metal carbonate, at a higher temperature.
<I> Example: </I> 25.6 parts of 1-chloro-2-nrethylantbrachinone, 34.3 parts of 1,4-monobenzoyldiämirroanthrachirron, 20 parts of anhydrous sodium carbonate, 1 part of copper acetate and 350 parts of nitrobenzene are 3 hours heated to boiling. The reaction product, which crystallizes out in needles, is separated out cold by filtration.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH208544T | 1938-07-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH208544A true CH208544A (en) | 1940-02-15 |
Family
ID=4446115
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH208544D CH208544A (en) | 1938-07-20 | 1938-07-20 | Process for the production of a nitrogen-containing condensation product. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH208544A (en) |
-
1938
- 1938-07-20 CH CH208544D patent/CH208544A/en unknown
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