GB901059A - Improvements in the production of 1,4-diaminoanthraquinone-2,3-dinitrile - Google Patents
Improvements in the production of 1,4-diaminoanthraquinone-2,3-dinitrileInfo
- Publication number
- GB901059A GB901059A GB2195460A GB2195460A GB901059A GB 901059 A GB901059 A GB 901059A GB 2195460 A GB2195460 A GB 2195460A GB 2195460 A GB2195460 A GB 2195460A GB 901059 A GB901059 A GB 901059A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sodium
- acid
- hydrogen peroxide
- reaction mixture
- saturated
- 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
- QUZJFTXRXJQLBH-UHFFFAOYSA-N 1,4-diamino-9,10-dioxoanthracene-2,3-dicarbonitrile Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=C(C#N)C(C#N)=C2N QUZJFTXRXJQLBH-UHFFFAOYSA-N 0.000 title 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 4
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 abstract 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 abstract 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 abstract 2
- 239000007800 oxidant agent Substances 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- GBECUEIQVRDUKB-UHFFFAOYSA-M thallium monochloride Chemical compound [Tl]Cl GBECUEIQVRDUKB-UHFFFAOYSA-M 0.000 abstract 2
- 229910000497 Amalgam Inorganic materials 0.000 abstract 1
- 239000004160 Ammonium persulphate Substances 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 abstract 1
- 229940010552 ammonium molybdate Drugs 0.000 abstract 1
- 235000018660 ammonium molybdate Nutrition 0.000 abstract 1
- 239000011609 ammonium molybdate Substances 0.000 abstract 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 abstract 1
- 235000019395 ammonium persulphate Nutrition 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 abstract 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 229940083542 sodium Drugs 0.000 abstract 1
- 229960001922 sodium perborate Drugs 0.000 abstract 1
- 229940045872 sodium percarbonate Drugs 0.000 abstract 1
- LJRGBERXYNQPJI-UHFFFAOYSA-M sodium;3-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC(S([O-])(=O)=O)=C1 LJRGBERXYNQPJI-UHFFFAOYSA-M 0.000 abstract 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 abstract 1
- 229910052716 thallium Inorganic materials 0.000 abstract 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 abstract 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
-
- 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
- C09B1/22—Dyes with unsubstituted amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB53744A DE1108704B (de) | 1959-06-25 | 1959-06-25 | Verfahren zur Herstellung von 1, 4-Diaminoanthrachinon-2, 3-dinitril |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB901059A true GB901059A (en) | 1962-07-11 |
Family
ID=6970366
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2195460A Expired GB901059A (en) | 1959-06-25 | 1960-06-23 | Improvements in the production of 1,4-diaminoanthraquinone-2,3-dinitrile |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE592155A (enrdf_load_stackoverflow) |
| CH (1) | CH385246A (enrdf_load_stackoverflow) |
| DE (1) | DE1108704B (enrdf_load_stackoverflow) |
| GB (1) | GB901059A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0023645A1 (de) * | 1979-08-07 | 1981-02-11 | Bayer Ag | Verfahren zur Herstellung von 1,4-Diamino-2,3-dicyanoanthrachinonen |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2066281B (en) | 1979-10-26 | 1983-05-25 | Sumitomo Chemical Co | Anthraquinone dye intermediate |
| DE3003656A1 (de) * | 1980-02-01 | 1981-08-06 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von 1,4-diamo-2,3-dicyano-anthrachinon |
| US4519947A (en) * | 1982-10-04 | 1985-05-28 | Sumitomo Chemical Co., Ltd. | Process for producing anthraquinone compounds |
| CH660877A5 (de) * | 1984-10-26 | 1987-05-29 | Ciba Geigy Ag | Verfahren zur herstellung von 1,4-diamino-2,3-dicyanoanthrachinon. |
| JPH0721114B2 (ja) * | 1985-12-10 | 1995-03-08 | 住友化学工業株式会社 | アントラキノン化合物の製造方法 |
-
0
- BE BE592155D patent/BE592155A/xx unknown
-
1959
- 1959-06-25 DE DEB53744A patent/DE1108704B/de active Pending
-
1960
- 1960-05-31 CH CH623160A patent/CH385246A/de unknown
- 1960-06-23 GB GB2195460A patent/GB901059A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0023645A1 (de) * | 1979-08-07 | 1981-02-11 | Bayer Ag | Verfahren zur Herstellung von 1,4-Diamino-2,3-dicyanoanthrachinonen |
Also Published As
| Publication number | Publication date |
|---|---|
| BE592155A (enrdf_load_stackoverflow) | |
| CH385246A (de) | 1964-12-15 |
| DE1108704B (de) | 1961-06-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Johnson et al. | Polarographic Reduction of Oxygen in Dimethylsulfoxide. | |
| DK0822920T3 (da) | Fremgangsmåde til fremstilling af en chlordioxidholdig desinfektionsopløsning til vandrensning | |
| GB901059A (en) | Improvements in the production of 1,4-diaminoanthraquinone-2,3-dinitrile | |
| Watts et al. | The thermochemical characterization of sodium dithionite, flavin mononucleotide, flavin-adenine dinucleotide and methyl and benzyl viologens as low-potential reductants for biological systems | |
| Mushran et al. | Mechanism of oxidations by chloramine-T. Part I. Oxidation of α-hydroxy-acids | |
| Mahadevappa et al. | Kinetics and mechanism of oxidation of allyl alchohol by chloramine-T in hydrochloric acid medium | |
| GB834514A (en) | Improvements in or relating to the preparation of potassium monopersulphate | |
| ES452324A1 (es) | Un procedimiento mejorado para tenir fibras textiles de al- godon o de celulosa regenerada. | |
| Brown et al. | A note on the preparation of chlorine gas containing Cl36 | |
| GB891094A (en) | Improvements in and relating to per-compounds | |
| Mahadevappa et al. | Estimation of thiosemicarbazide with chloramine-T | |
| GB1438901A (en) | Peroxide oxidation of impurities in aqueous effluent | |
| GB1513637A (en) | Process for the preparation of azodicarbonamide | |
| Bailar | The oxidation states of silver | |
| GB697196A (en) | Improvements in or relating to electroplating of basis metal with zinc | |
| GB1356892A (en) | Process for the manufacture of dialkylphosphine oxides | |
| GB1141956A (en) | 2-phenylbenzoxazoles and cosmetic preparations containing them | |
| GB1469907A (en) | Method for preparing bis-2-pyridyl-1-oxide- disulphide | |
| Kendall et al. | The mechanism of oxidation-reduction potential: The oxidation-reduction potential of cysteine and cystine | |
| GB619206A (en) | Diacetylenic diamines | |
| Sanehi et al. | Kinetics of the Oxidation of Ethylene Diamine Tetra Acetic Acid by Chloramine-T | |
| GB868339A (en) | Improvements in oxidation processes with chlorites | |
| GB877232A (en) | Improvements in or relating to the preparation of permonosulphates | |
| Rich et al. | A bromate clock reaction: The formation of purple tris (diphosphato) manganate (III) | |
| Matsui et al. | Polarographic Studies of the Anodic Oxidation of Mercury. I. Anodic Waves of Ammonia and Several Amines in N, N-Dimethylformamide |