DE216715C - - Google Patents
Info
- Publication number
- DE216715C DE216715C DENDAT216715D DE216715DA DE216715C DE 216715 C DE216715 C DE 216715C DE NDAT216715 D DENDAT216715 D DE NDAT216715D DE 216715D A DE216715D A DE 216715DA DE 216715 C DE216715 C DE 216715C
- Authority
- DE
- Germany
- Prior art keywords
- weight
- parts
- methylanthraquinone
- bromine
- derivative
- 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
- NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical class C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 claims description 18
- RBGUKBSLNOTVCD-UHFFFAOYSA-N 1-methylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C RBGUKBSLNOTVCD-UHFFFAOYSA-N 0.000 claims description 13
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 12
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 229960000583 acetic acid Drugs 0.000 claims description 5
- 239000012362 glacial acetic acid Substances 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003963 dichloro group Chemical group Cl* 0.000 claims 3
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims 2
- -1 bromine compound Chemical class 0.000 claims 1
- 238000005660 chlorination reaction Methods 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- 239000013078 crystal Substances 0.000 claims 1
- 239000000706 filtrate Substances 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 239000010931 gold Substances 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 238000000227 grinding Methods 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
- 238000010626 work up procedure Methods 0.000 claims 1
- QPAGCTACMMYJIO-UHFFFAOYSA-N 1,2-dihydroxy-3-methylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=C(C)C(O)=C2O QPAGCTACMMYJIO-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000950 dibromo group Chemical group Br* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/26—Quinones containing groups having oxygen atoms singly bound to carbon atoms
- C07C50/34—Quinones containing groups having oxygen atoms singly bound to carbon atoms the quinoid structure being part of a condensed ring system having three rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C50/00—Quinones
- C07C50/24—Quinones containing halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE216715C true DE216715C (enrdf_load_stackoverflow) |
Family
ID=478096
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT216715D Active DE216715C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE216715C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT216715D patent/DE216715C/de active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE216715C (enrdf_load_stackoverflow) | ||
DE1618207A1 (de) | Partielle Chlorierung von Acetessigsaeure-monoalkylamiden | |
DE865925C (de) | Verfahren zur Herstellung von basischen Polymethinfarbstoffen | |
DE260898C (enrdf_load_stackoverflow) | ||
DE251480C (enrdf_load_stackoverflow) | ||
DE98760C (enrdf_load_stackoverflow) | ||
DE255121C (enrdf_load_stackoverflow) | ||
DE1645890A1 (de) | Verfahren zur Herstellung substituierter epsilon-Caprolactame | |
DE253683C (enrdf_load_stackoverflow) | ||
DE79960C (enrdf_load_stackoverflow) | ||
DE125094C (enrdf_load_stackoverflow) | ||
DE650049C (de) | Verfahren zur Darstellung halogenierter Pyridinabkoemmlinge | |
DE216071C (enrdf_load_stackoverflow) | ||
DE3431416A1 (de) | Verfahren zur herstellung von 2-hydroxy-5,6,7,8-tetrahydrocarbazol, die alkali- und erdalkalisalze des 2-hydroxy-5,6,7,8-tetrahydrocarbazols und deren verwendung | |
DE120899C (enrdf_load_stackoverflow) | ||
DE580647C (de) | Verfahren zur Darstellung von chlor- und stickstoffhaltigen Anthrachinonderivaten | |
DE1470071C (de) | Verfahren zur Herstellung von N Halo gen N phenyl amidinen | |
DE586068C (de) | Verfahren zur Darstellung von stickstoffhaltigen Derivaten des Anthracens | |
DE260905C (enrdf_load_stackoverflow) | ||
DE290209C (enrdf_load_stackoverflow) | ||
DE211967C (enrdf_load_stackoverflow) | ||
DE575948C (de) | Verfahren zur Herstellung von Kondensationsprodukten | |
DE659483C (de) | Verfahren zur Darstellung von (1-Phenyl-2, 3-dimethyl-5-pyrazolonyl) -isopentylketon | |
DE114262C (enrdf_load_stackoverflow) | ||
DE264943C (enrdf_load_stackoverflow) |