GB1405637A - Production of 1-amino-4-hydroxyanthraquinones substituted in the 2-and or 3-positions - Google Patents
Production of 1-amino-4-hydroxyanthraquinones substituted in the 2-and or 3-positionsInfo
- Publication number
- GB1405637A GB1405637A GB5793272A GB5793272A GB1405637A GB 1405637 A GB1405637 A GB 1405637A GB 5793272 A GB5793272 A GB 5793272A GB 5793272 A GB5793272 A GB 5793272A GB 1405637 A GB1405637 A GB 1405637A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bromine
- chlorine
- amino
- substituted
- nitrobenzoyl
- 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
- AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical group O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 title 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 3
- 229910052794 bromium Inorganic materials 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- -1 3-substituted-1-amino-4-hydroxy anthraquinones Chemical class 0.000 abstract 2
- 239000005711 Benzoic acid Substances 0.000 abstract 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 abstract 2
- 229910052796 boron Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 238000006396 nitration reaction Methods 0.000 abstract 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 abstract 2
- 235000011149 sulphuric acid Nutrition 0.000 abstract 2
- 239000001117 sulphuric acid Substances 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 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 abstract 1
- 239000004327 boric acid Substances 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
- C09B1/503—Amino-hydroxy-anthraquinones; Ethers and esters thereof unsubstituted amino-hydroxy anthraquinone
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 |
|---|---|---|---|
| DE19712163059 DE2163059C3 (de) | 1971-12-18 | Verfahren zur Herstellung von in 2-Stellung substituierten 1-Amino-4hydroxyanthrachinonen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1405637A true GB1405637A (en) | 1975-09-10 |
Family
ID=5828503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5793272A Expired GB1405637A (en) | 1971-12-18 | 1972-12-15 | Production of 1-amino-4-hydroxyanthraquinones substituted in the 2-and or 3-positions |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3880892A (enExample) |
| JP (1) | JPS547018B2 (enExample) |
| CH (1) | CH574908A5 (enExample) |
| CS (1) | CS176217B2 (enExample) |
| DD (1) | DD100936A5 (enExample) |
| FR (1) | FR2165599A5 (enExample) |
| GB (1) | GB1405637A (enExample) |
| IT (1) | IT974053B (enExample) |
| SU (1) | SU457212A3 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0044893B1 (en) * | 1980-07-29 | 1984-09-19 | Imperial Chemical Industries Plc | Anthraquinone compounds and process for their preparation |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH658856A5 (de) * | 1984-05-29 | 1986-12-15 | Ciba Geigy Ag | Verfahren zur herstellung von organischen, aromatischen und heterocyclischen hydroxy-verbindungen. |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1798156A (en) * | 1928-02-06 | 1931-03-31 | Newport Chemical Corp | 1-amino-2-chloro-4-hydroxy anthraquinone and process of preparing the same |
| US1867069A (en) * | 1929-02-14 | 1932-07-12 | Gen Aniline Works Inc | Manufacture of 1-hydroxy- or 1-alkoxy anthraquinone-3-carboxylic acids |
-
1972
- 1972-12-12 CH CH1805872A patent/CH574908A5/xx not_active IP Right Cessation
- 1972-12-13 IT IT54691/72A patent/IT974053B/it active
- 1972-12-14 CS CS8600A patent/CS176217B2/cs unknown
- 1972-12-15 SU SU1860621A patent/SU457212A3/ru active
- 1972-12-15 DD DD167586A patent/DD100936A5/xx unknown
- 1972-12-15 GB GB5793272A patent/GB1405637A/en not_active Expired
- 1972-12-18 JP JP12633172A patent/JPS547018B2/ja not_active Expired
- 1972-12-18 FR FR7245123A patent/FR2165599A5/fr not_active Expired
-
1974
- 1974-12-15 US US315473*[A patent/US3880892A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0044893B1 (en) * | 1980-07-29 | 1984-09-19 | Imperial Chemical Industries Plc | Anthraquinone compounds and process for their preparation |
Also Published As
| Publication number | Publication date |
|---|---|
| IT974053B (it) | 1974-06-20 |
| US3880892A (en) | 1975-04-29 |
| JPS4868626A (enExample) | 1973-09-19 |
| DE2163059B2 (de) | 1975-06-12 |
| CH574908A5 (enExample) | 1976-04-30 |
| FR2165599A5 (enExample) | 1973-08-03 |
| DD100936A5 (enExample) | 1973-10-12 |
| SU457212A3 (ru) | 1975-01-15 |
| JPS547018B2 (enExample) | 1979-04-03 |
| CS176217B2 (enExample) | 1977-06-30 |
| DE2163059A1 (de) | 1973-06-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |