DE2457703C2 - Verfahren zur Herstellung von 4,4', 7,7'-Tetrachlorthioindigo in Pigmentform - Google Patents
Verfahren zur Herstellung von 4,4', 7,7'-Tetrachlorthioindigo in PigmentformInfo
- Publication number
- DE2457703C2 DE2457703C2 DE2457703A DE2457703A DE2457703C2 DE 2457703 C2 DE2457703 C2 DE 2457703C2 DE 2457703 A DE2457703 A DE 2457703A DE 2457703 A DE2457703 A DE 2457703A DE 2457703 C2 DE2457703 C2 DE 2457703C2
- Authority
- DE
- Germany
- Prior art keywords
- tetrachlorothioindigo
- acid
- hydroxy
- dichloro
- thionaphthene
- 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
- 238000000034 method Methods 0.000 title claims description 15
- 239000000049 pigment Substances 0.000 title claims description 11
- KZFMOINJHMONLW-FOCLMDBBSA-N (2e)-4,7-dichloro-2-(4,7-dichloro-3-oxo-1-benzothiophen-2-ylidene)-1-benzothiophen-3-one Chemical compound S\1C(C(=CC=C2Cl)Cl)=C2C(=O)C/1=C1/C(=O)C(C(Cl)=CC=C2Cl)=C2S1 KZFMOINJHMONLW-FOCLMDBBSA-N 0.000 title claims description 8
- 238000007254 oxidation reaction Methods 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- -1 Transition metal salts Chemical class 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 3
- 238000004040 coloring Methods 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 150000004679 hydroxides Chemical class 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910000365 copper sulfate Inorganic materials 0.000 claims description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 2
- 239000012074 organic phase Substances 0.000 claims description 2
- 239000004033 plastic Substances 0.000 claims description 2
- 229920003023 plastic Polymers 0.000 claims description 2
- 230000001133 acceleration Effects 0.000 claims 1
- 150000002696 manganese Chemical class 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 9
- 230000007935 neutral effect Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- AIFKBFKJMQTYAM-UHFFFAOYSA-N 2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-phenylpentanoic acid Chemical compound CC(C)(C)OC(=O)NC(C(O)=O)CCCC1=CC=CC=C1 AIFKBFKJMQTYAM-UHFFFAOYSA-N 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000012874 anionic emulsifier Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000009969 flowable effect Effects 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- SAKPHDMJHWIWMI-UHFFFAOYSA-N 2-(2,5-dichlorophenyl)-2-sulfanylacetyl chloride Chemical compound ClC(=O)C(S)C1=CC(Cl)=CC=C1Cl SAKPHDMJHWIWMI-UHFFFAOYSA-N 0.000 description 1
- UGDAWAQEKLURQI-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethanol;hydrate Chemical compound O.OCCOCCO UGDAWAQEKLURQI-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical class [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- OENLEHTYJXMVBG-UHFFFAOYSA-N pyridine;hydrate Chemical compound [OH-].C1=CC=[NH+]C=C1 OENLEHTYJXMVBG-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-N sodium polysulfide Chemical compound [Na+].S HYHCSLBZRBJJCH-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000001238 wet grinding Methods 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
- C09B7/00—Indigoid dyes
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2457703A DE2457703C2 (de) | 1974-12-06 | 1974-12-06 | Verfahren zur Herstellung von 4,4', 7,7'-Tetrachlorthioindigo in Pigmentform |
GB4226175A GB1463229A (en) | 1974-12-06 | 1975-10-15 | Process for the preparation of 4,4,7,7-tetrachlorthioindigo in pigment form |
CH1557675A CH592720A5 (en, 2012) | 1974-12-06 | 1975-12-01 | |
JP50143418A JPS5182288A (en) | 1974-12-06 | 1975-12-04 | Ganryonokatachino 4 4* 7 7* tetorakurorochioinjigono seizoho |
FR7537305A FR2293473A1 (fr) | 1974-12-06 | 1975-12-05 | Procede de production du 4,4'7,7'-tetrachloroindigo sous forme de pigment |
US06/163,851 US4299966A (en) | 1974-12-06 | 1980-06-27 | Process for the preparation of 4,4',7,7'-tetrachlorthioindigo in pigment form |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2457703A DE2457703C2 (de) | 1974-12-06 | 1974-12-06 | Verfahren zur Herstellung von 4,4', 7,7'-Tetrachlorthioindigo in Pigmentform |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2457703A1 DE2457703A1 (de) | 1976-06-10 |
DE2457703C2 true DE2457703C2 (de) | 1984-09-20 |
Family
ID=5932688
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2457703A Expired DE2457703C2 (de) | 1974-12-06 | 1974-12-06 | Verfahren zur Herstellung von 4,4', 7,7'-Tetrachlorthioindigo in Pigmentform |
Country Status (6)
Country | Link |
---|---|
US (1) | US4299966A (en, 2012) |
JP (1) | JPS5182288A (en, 2012) |
CH (1) | CH592720A5 (en, 2012) |
DE (1) | DE2457703C2 (en, 2012) |
FR (1) | FR2293473A1 (en, 2012) |
GB (1) | GB1463229A (en, 2012) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2916400A1 (de) | 1979-04-23 | 1980-11-13 | Basf Ag | Verfahren zur herstellung von lasierenden pigmentformen des 4,4',7,7'-tetrachlorthioindigo |
DE3101873A1 (de) * | 1981-01-22 | 1982-08-26 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von farbstarken 4,4',7,7'-tetrachlorthioindigopigmenten |
DE3121980A1 (de) * | 1981-06-03 | 1982-12-30 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von 4,7-dichlor-3-hydroxythionaphthen |
JPS58183900U (ja) * | 1982-06-02 | 1983-12-07 | 日本工機 株式会社 | 伸縮可能な柵体 |
JPS596200U (ja) * | 1982-07-06 | 1984-01-14 | 日本工機株式会社 | 伸縮自在な柵体 |
DE3324879A1 (de) * | 1983-07-09 | 1985-01-17 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung eines pigments auf basis 4,4',7,7'-tetrachlorthioindigo |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1710981A (en) * | 1926-05-29 | 1929-04-30 | Grasselli Dyestuff Corp | Vat dyestuffs and process of preparing the same |
US2029714A (en) * | 1930-02-22 | 1936-02-04 | Gen Aniline Works Inc | Thioindigo dyestuff preparations and a process of preparing them |
US1938054A (en) * | 1932-01-11 | 1933-12-05 | Gen Aniline Works Inc | Indigoid dyestuff |
US2804464A (en) * | 1954-06-28 | 1957-08-27 | American Cyanamid Co | Preparation of thioindigoid dyestuffs |
-
1974
- 1974-12-06 DE DE2457703A patent/DE2457703C2/de not_active Expired
-
1975
- 1975-10-15 GB GB4226175A patent/GB1463229A/en not_active Expired
- 1975-12-01 CH CH1557675A patent/CH592720A5/xx not_active IP Right Cessation
- 1975-12-04 JP JP50143418A patent/JPS5182288A/ja active Granted
- 1975-12-05 FR FR7537305A patent/FR2293473A1/fr active Granted
-
1980
- 1980-06-27 US US06/163,851 patent/US4299966A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US4299966A (en) | 1981-11-10 |
DE2457703A1 (de) | 1976-06-10 |
CH592720A5 (en, 2012) | 1977-11-15 |
FR2293473B1 (en, 2012) | 1980-01-11 |
JPS5182288A (en) | 1976-07-19 |
FR2293473A1 (fr) | 1976-07-02 |
GB1463229A (en) | 1977-02-02 |
JPS5747694B2 (en, 2012) | 1982-10-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
D2 | Grant after examination | ||
8364 | No opposition during term of opposition | ||
8339 | Ceased/non-payment of the annual fee |