SU457212A3 - Способ получени замещенных 1амино-4-оксиантрахинона - Google Patents
Способ получени замещенных 1амино-4-оксиантрахинонаInfo
- Publication number
- SU457212A3 SU457212A3 SU1860621A SU1860621A SU457212A3 SU 457212 A3 SU457212 A3 SU 457212A3 SU 1860621 A SU1860621 A SU 1860621A SU 1860621 A SU1860621 A SU 1860621A SU 457212 A3 SU457212 A3 SU 457212A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- weight
- acid
- amino
- hours
- oleum
- Prior art date
Links
- AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 title 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 8
- 239000004327 boric acid Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- MFAVJLWGAQYYNX-UHFFFAOYSA-N 1-amino-2-chloro-4-hydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC(Cl)=C2N MFAVJLWGAQYYNX-UHFFFAOYSA-N 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 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 1
- BVEIKFLZWBDLJG-UHFFFAOYSA-N 1-butylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2CCCC BVEIKFLZWBDLJG-UHFFFAOYSA-N 0.000 description 1
- INPHIYULSHLAHR-UHFFFAOYSA-N 1-pentylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2CCCCC INPHIYULSHLAHR-UHFFFAOYSA-N 0.000 description 1
- RITAQDHCJBLSSL-UHFFFAOYSA-N 2-(4-chloro-3-nitrobenzoyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 RITAQDHCJBLSSL-UHFFFAOYSA-N 0.000 description 1
- YWECCEXWKFHHQJ-UHFFFAOYSA-N 2-(4-chlorobenzoyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)C1=CC=C(Cl)C=C1 YWECCEXWKFHHQJ-UHFFFAOYSA-N 0.000 description 1
- ICBCRGZLADYRFP-UHFFFAOYSA-N 2-benzoyl-3-butylbenzoic acid Chemical compound CCCCC1=CC=CC(C(O)=O)=C1C(=O)C1=CC=CC=C1 ICBCRGZLADYRFP-UHFFFAOYSA-N 0.000 description 1
- XTFDFHAXYIQCLL-UHFFFAOYSA-N 2-benzoyl-3-pentylbenzoic acid Chemical compound CCCCCC1=CC=CC(C(O)=O)=C1C(=O)C1=CC=CC=C1 XTFDFHAXYIQCLL-UHFFFAOYSA-N 0.000 description 1
- -1 3-Nitro-4-bromobenzoylbenzoic acid Chemical compound 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 235000005811 Viola adunca Nutrition 0.000 description 1
- 240000009038 Viola odorata Species 0.000 description 1
- 235000013487 Viola odorata Nutrition 0.000 description 1
- 235000002254 Viola papilionacea Nutrition 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification 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
- 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 |
|---|---|
| SU457212A3 true SU457212A3 (ru) | 1975-01-15 |
Family
ID=5828503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1860621A SU457212A3 (ru) | 1971-12-18 | 1972-12-15 | Способ получени замещенных 1амино-4-оксиантрахинона |
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) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3069220D1 (en) * | 1980-07-29 | 1984-10-25 | Ici Plc | Anthraquinone compounds and process for their preparation |
| 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
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 |
| GB1405637A (en) | 1975-09-10 |
| JPS547018B2 (enExample) | 1979-04-03 |
| CS176217B2 (enExample) | 1977-06-30 |
| DE2163059A1 (de) | 1973-06-20 |
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