DE3337675C2 - - Google Patents
Info
- Publication number
- DE3337675C2 DE3337675C2 DE19833337675 DE3337675A DE3337675C2 DE 3337675 C2 DE3337675 C2 DE 3337675C2 DE 19833337675 DE19833337675 DE 19833337675 DE 3337675 A DE3337675 A DE 3337675A DE 3337675 C2 DE3337675 C2 DE 3337675C2
- Authority
- DE
- Germany
- Prior art keywords
- aqueous
- reduction
- formaldehyde
- catalyst
- mononitroviolanthrone
- 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 - Lifetime
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 7
- -1 compound sodium hydroxide Chemical class 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 2
- 230000001476 alcoholic effect Effects 0.000 claims 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims 1
- 239000000243 solution Substances 0.000 description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- VZMULMSIWMLZLC-UHFFFAOYSA-N 2-aminoanthra[9,1,2-cde]benzo[rst]pentaphene-5,10-dione Chemical compound C12=C3C4=CC=C2C2=CC=CC=C2C(=O)C1=CC=C3C1=CC=C2C(=O)C3=CC=C(N)C=C3C3=CC=C4C1=C32 VZMULMSIWMLZLC-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052979 sodium sulfide Inorganic materials 0.000 description 2
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 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 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical group [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 150000003112 potassium compounds Chemical class 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 239000002351 wastewater Substances 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/22—Dibenzanthrones; Isodibenzanthrones
- C09B3/30—Preparation from starting materials already containing the dibenzanthrone or isodibenzanthrone nucleus
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 |
---|---|---|---|
CH608482A CH653987A5 (de) | 1982-10-19 | 1982-10-19 | Verfahren zur herstellung von monoaminoviolanthron. |
Publications (2)
Publication Number | Publication Date |
---|---|
DE3337675A1 DE3337675A1 (de) | 1984-04-26 |
DE3337675C2 true DE3337675C2 (en, 2012) | 1992-01-02 |
Family
ID=4304005
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19833337675 Granted DE3337675A1 (de) | 1982-10-19 | 1983-10-17 | Verfahren zur herstellung von monoaminoviolanthron |
Country Status (2)
Country | Link |
---|---|
CH (1) | CH653987A5 (en, 2012) |
DE (1) | DE3337675A1 (en, 2012) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102660130B (zh) * | 2012-04-19 | 2014-05-07 | 徐州开达精细化工有限公司 | 生产还原直接黑bcn原染料的方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3073849A (en) * | 1959-11-25 | 1963-01-15 | Allied Chem | Process for producing direct black vat dyestuffs |
-
1982
- 1982-10-19 CH CH608482A patent/CH653987A5/de not_active IP Right Cessation
-
1983
- 1983-10-17 DE DE19833337675 patent/DE3337675A1/de active Granted
Also Published As
Publication number | Publication date |
---|---|
DE3337675A1 (de) | 1984-04-26 |
CH653987A5 (de) | 1986-01-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE3228881C2 (de) | Verfahren zur Herstellung von C↓3↓-C↓5↓-Alkoholen | |
DD156966A5 (de) | Verfahren zur herstellung von hochreinem monoethylenglykol | |
DE2054601C3 (de) | Verfahren zur Herstellung von zweiwertigen Alkoholen | |
EP0088275B1 (de) | Verfahren zur Herstellung von Trimethylolpropan | |
DE2115551B2 (de) | Verfahren zur Herstellung von aromatischen Hydroxyaldehyden | |
DE3337675C2 (en, 2012) | ||
DE3106476A1 (de) | Verfahren zur herstellung von trioxan | |
DE1014089B (de) | Verfahren zur Herstellung von 2,2-Dimethylpropandiol-(1,3) | |
DE2216974C3 (de) | Verfahren zur Herstellung höhermolekularer ungesättigter Ketone | |
DE3337707C2 (en, 2012) | ||
DE2209458A1 (de) | Verfahren zur Herstellung von 1,4-Dithiol-2,3-butandiol. ^Anm: AvonProdücts, Inc., New York (V.StA.) | |
CH631146A5 (de) | Verfahren zur herstellung von 2,6-dimethoxy-4-(quaternaeren-alkyl)phenolen. | |
DE4023255A1 (de) | Verfahren zur herstellung von glykolen, insbesondere propylenglykol aus formaldehyd | |
AT164041B (de) | Verfahren zur Herstellung antiseptischer Lösungen | |
DE705274C (de) | Verfahren zur Herstellung von Oxyoxoverbindungen | |
DE891693C (de) | Verfahren zur Herstellung schwefelhaltiger Verbindungen | |
DE930205C (de) | Verfahren zur Herstellung neuer Oxymethylharnstoffe | |
DE1001988C2 (de) | Verfahren zur Herstellung niederer Alkylaether von Isonicotinsaeure-oxymethylamid | |
DE2163854C3 (de) | Verfahren zur Herstellung von N-Hydroxymethyl-4-oxotetrahydro-1,3,5-oxadiazinen | |
DE765787C (de) | Verfahren zur Herstellung von Umsetzungsprodukten von Formaldehyd mit Blausaeure | |
DE3241446A1 (de) | Verfahren zur herstellung nahezu farbloser textilausruestungsmittel auf glyoxalbasis | |
DE2263881A1 (de) | Verfahren zur herstellung von carvon | |
DE1171437B (de) | Verfahren zur Herstellung von Imidazolidinonen | |
DE2722957B2 (de) | Verfahren zur Herstellung von 13-Diamino-2,2-dimethyI-propan | |
DE2337196C3 (de) | Verfahren zur Herstellung hochkonzentrierter Gerbstoff-Formulierungen |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
8125 | Change of the main classification |
Ipc: C09B 3/22 |
|
D2 | Grant after examination | ||
8364 | No opposition during term of opposition | ||
8339 | Ceased/non-payment of the annual fee |