DE122852C - - Google Patents
Info
- Publication number
- DE122852C DE122852C DENDAT122852D DE122852DA DE122852C DE 122852 C DE122852 C DE 122852C DE NDAT122852 D DENDAT122852 D DE NDAT122852D DE 122852D A DE122852D A DE 122852DA DE 122852 C DE122852 C DE 122852C
- Authority
- DE
- Germany
- Prior art keywords
- carbazole
- anthracene
- nitrosocarbazole
- solution
- nitrous acid
- 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
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 48
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 40
- QQIBDMGORGPLPU-UHFFFAOYSA-N 1-nitroso-9h-carbazole Chemical compound C12=CC=CC=C2NC2=C1C=CC=C2N=O QQIBDMGORGPLPU-UHFFFAOYSA-N 0.000 claims description 13
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 claims description 11
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 238000000746 purification Methods 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 10
- 150000001716 carbazoles Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000011280 coal tar Substances 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000002832 nitroso derivatives Chemical class 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- LZDSILRDTDCIQT-UHFFFAOYSA-N dinitrogen trioxide Chemical compound [O-][N+](=O)N=O LZDSILRDTDCIQT-UHFFFAOYSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WFTICIXFISZPCW-UHFFFAOYSA-N 9h-carbazole;potassium Chemical compound [K].C1=CC=C2C3=CC=CC=C3NC2=C1 WFTICIXFISZPCW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- XLXWAFSNXPPDAB-UHFFFAOYSA-N anthracene;9h-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1.C1=CC=CC2=CC3=CC=CC=C3C=C21 XLXWAFSNXPPDAB-UHFFFAOYSA-N 0.000 description 1
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
- C07C7/17—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound with acids or sulfur oxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Indole Compounds (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE122852C true DE122852C (en:Method) |
Family
ID=391744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT122852D Active DE122852C (en:Method) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE122852C (en:Method) |
-
0
- DE DENDAT122852D patent/DE122852C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE122852C (en:Method) | ||
DE2258484C3 (de) | Verfahren zum Reinigen von rohem 2-Mercaptobenzothiazol | |
DE2022569A1 (de) | Verfahren zur Reinigung von rohem 2-Mercaptobenzothiazol | |
DE68909118T2 (de) | Verfahren zur Ausscheidung von 2,6-Dimethylnaphthalin. | |
DE888177C (de) | Verfahren zur Aufarbeitung von Teer-Rueckstaenden | |
AT10002B (de) | Verfahren zur Reinigung von Rohanthracen unter Wiedergewinnung des Reinigungsmittels. | |
DE1025875B (de) | Verfahren zur Abtrennung von Begleitstoffen aus kristallinen Stoffen | |
EP0247456B1 (de) | Verfahren zur Reinigung von 1-Amino-5-hydroxynaphthalin enthaltendem 1,5-Diaminonaphthalin | |
DE128853C (en:Method) | ||
DE42053C (de) | Verfahren zur Reinigung des Rohanthracens | |
DE726546C (de) | Verfahren zur Gewinnung von 1, 12-Benzoperylen oder Coronen oder beiden | |
AT116066B (de) | Verfahren zur Reinigung von Rohmontanwachs. | |
DE842047C (de) | Verfahren zur Herstellung von Fumarsaeure aus Maleinsaeureanhydrid enthaltenden Gasen, die durch katalytische Dampfphasenoxydation von organischen Verbindungen erhalten werden | |
DE551028C (de) | Verfahren zur Herstellung von reinem Anthracen | |
EP0043031B1 (de) | Verfahren zur Gewinnung von reinen Anilin-Verbindungen | |
DE2944916A1 (de) | Verfahren zur abtrennung von metallen aus russ | |
EP0218005B1 (de) | Eintopfverfahren zur Herstellung von 2-Acetaminonaphthalin-6-sulfonsäure hoher Reinheit | |
DE918208C (de) | Verfahren zur Herstellung von Acrylsaeurenitril | |
AT48615B (de) | Verfahren zur Gewinnung von Indol aus Steinkohlenteerölen. | |
DE124150C (en:Method) | ||
DE299015C (en:Method) | ||
DE223304A (en:Method) | ||
DE588283C (de) | Verfahren zur Herstellung nicht benzolartiger ungesaettigter Kohlenwasserstoffe hoeheren Molekulargewichts aus Acetylen | |
DE492228C (de) | Verwertung von organischen Stoffen | |
AT162632B (de) | Verfahren zur Reinigung von Rohmontanwachs |