DE218476C - - Google Patents
Info
- Publication number
- DE218476C DE218476C DENDAT218476D DE218476DA DE218476C DE 218476 C DE218476 C DE 218476C DE NDAT218476 D DENDAT218476 D DE NDAT218476D DE 218476D A DE218476D A DE 218476DA DE 218476 C DE218476 C DE 218476C
- Authority
- DE
- Germany
- Prior art keywords
- anthraquinone
- quinoline
- melting point
- sulfuric acid
- class
- 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.)
- Active
Links
- 230000000802 nitrating effect Effects 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 2
- -1 mononitroanthraquinone quinolines Chemical class 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 6
- 150000004056 anthraquinones Chemical class 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 238000006396 nitration reaction Methods 0.000 description 4
- 229910017604 nitric acid Inorganic materials 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 3
- 150000002828 nitro derivatives Chemical class 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- DZHDFIWOPAVEOZ-UHFFFAOYSA-N anthracene-9,10-dione;quinoline Chemical class N1=CC=CC2=CC=CC=C21.C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 DZHDFIWOPAVEOZ-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- JROURLWMOZCGJV-UHFFFAOYSA-N alizarin blue Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C1=CC=CN=C1C(O)=C2O JROURLWMOZCGJV-UHFFFAOYSA-N 0.000 description 1
- 229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE218476C true DE218476C (cs) |
Family
ID=479695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT218476D Active DE218476C (cs) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE218476C (cs) |
-
0
- DE DENDAT218476D patent/DE218476C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE218476C (cs) | ||
| DE203083C (cs) | ||
| DE280712C (cs) | ||
| DE514415C (de) | Verfahren zur Einfuehrung von Aldehydgruppen in sauerstoffhaltige cyklische Verbindungen | |
| DE567755C (de) | Verfahren zur Darstellung von Anthrachinonderivaten | |
| DE229394C (cs) | ||
| DE171939C (cs) | ||
| DE360530C (de) | Verfahren zur Einfuehrung von Arylaminogruppen in Aminoanthrachinone | |
| DE180157C (cs) | ||
| DE1260656B (de) | Verfahren zur Herstellung von 1, 4-Diaminoanthrachinon-2, 3-dicarbonsaeureimid-Dispersionsfarbstoffen | |
| DE194197C (cs) | ||
| DE280092C (cs) | ||
| DE147851C (cs) | ||
| DE234742C (cs) | ||
| DE450999C (de) | Verfahren zur Darstellung von Kuepenfarbstoffen der Dibenzanthronreihe | |
| DE341886C (cs) | ||
| CH262959A (de) | Verfahren zur Herstellung des neuen a-(Benzthiazyl-(2))-B-(benzimidazyl-(2))-äthylens. | |
| DE286094C (cs) | ||
| DE215294C (cs) | ||
| DE251845C (cs) | ||
| DE430631C (de) | Verfahren zur Darstellung von Beizenfarbstoffen der Phenanthrenchinonreihe | |
| DE415318C (de) | Verfahren zur Herstellung von 4-Arylamino-1-arylimino-2-naphthochinonen | |
| DE67115C (de) | Verfahren und Darstellung von o-Tolylrosindulin | |
| DE282374C (cs) | ||
| DE237546C (cs) |