DE2740403C2 - - Google Patents
Info
- Publication number
- DE2740403C2 DE2740403C2 DE2740403A DE2740403A DE2740403C2 DE 2740403 C2 DE2740403 C2 DE 2740403C2 DE 2740403 A DE2740403 A DE 2740403A DE 2740403 A DE2740403 A DE 2740403A DE 2740403 C2 DE2740403 C2 DE 2740403C2
- Authority
- DE
- Germany
- Prior art keywords
- dinitroanthraquinone
- acid
- mixed acid
- nitric acid
- temperature
- 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
- 239000002253 acid Substances 0.000 claims description 39
- XVMVHWDCRFNPQR-UHFFFAOYSA-N 1,5-dinitroanthracene-9,10-dione Chemical compound O=C1C=2C([N+](=O)[O-])=CC=CC=2C(=O)C2=C1C=CC=C2[N+]([O-])=O XVMVHWDCRFNPQR-UHFFFAOYSA-N 0.000 claims description 35
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 28
- 239000000725 suspension Substances 0.000 claims description 28
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 27
- 229910017604 nitric acid Inorganic materials 0.000 claims description 27
- 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 claims description 20
- 150000004056 anthraquinones Chemical class 0.000 claims description 20
- NMNSBFYYVHREEE-UHFFFAOYSA-N 1,2-dinitroanthracene-9,10-dione Chemical class C1=CC=C2C(=O)C3=C([N+]([O-])=O)C([N+](=O)[O-])=CC=C3C(=O)C2=C1 NMNSBFYYVHREEE-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 239000013078 crystal Substances 0.000 claims description 5
- 238000010306 acid treatment Methods 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000000926 separation method Methods 0.000 description 18
- 239000002002 slurry Substances 0.000 description 15
- MBIJFIUDKPXMAV-UHFFFAOYSA-N 1,8-dinitroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC([N+]([O-])=O)=C2C(=O)C2=C1C=CC=C2[N+](=O)[O-] MBIJFIUDKPXMAV-UHFFFAOYSA-N 0.000 description 12
- 238000006396 nitration reaction Methods 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000012452 mother liquor Substances 0.000 description 8
- 238000005121 nitriding Methods 0.000 description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000002699 waste material Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000000802 nitrating effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- UQKJUEALIQRECQ-UHFFFAOYSA-N 1,6-dinitroanthracene-9,10-dione Chemical compound O=C1C2=CC([N+](=O)[O-])=CC=C2C(=O)C2=C1C=CC=C2[N+]([O-])=O UQKJUEALIQRECQ-UHFFFAOYSA-N 0.000 description 1
- YCANAXVBJKNANM-UHFFFAOYSA-N 1-nitroanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2[N+](=O)[O-] YCANAXVBJKNANM-UHFFFAOYSA-N 0.000 description 1
- OPXXCGAYBFDPHY-UHFFFAOYSA-N 2,6-dinitroanthracene-9,10-dione Chemical compound [O-][N+](=O)C1=CC=C2C(=O)C3=CC([N+](=O)[O-])=CC=C3C(=O)C2=C1 OPXXCGAYBFDPHY-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229940082150 encore Drugs 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical class C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/24—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings
- C07C225/26—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings
- C07C225/32—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings of condensed quinone ring systems formed by at least three rings
- C07C225/34—Amino anthraquinones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C46/00—Preparation of quinones
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 |
|---|---|---|---|
| JP10966976A JPS5334765A (en) | 1976-09-13 | 1976-09-13 | Isolation of 1,5-dinitroanthraquinone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2740403A1 DE2740403A1 (de) | 1978-03-16 |
| DE2740403C2 true DE2740403C2 (en, 2012) | 1987-07-23 |
Family
ID=14516156
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772740403 Granted DE2740403A1 (de) | 1976-09-13 | 1977-09-08 | Verfahren zur herstellung von 1,5-dinitroanthrachinon |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4158009A (en, 2012) |
| JP (1) | JPS5334765A (en, 2012) |
| CH (1) | CH638486A5 (en, 2012) |
| DE (1) | DE2740403A1 (en, 2012) |
| GB (1) | GB1564054A (en, 2012) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2909481A1 (de) * | 1979-03-10 | 1980-09-11 | Bayer Ag | Verfahren zur herstellung von 4,5-dinitro-1,8-dihydroxyanthrachinon |
| CN111454158A (zh) * | 2020-05-14 | 2020-07-28 | 九江富达实业有限公司 | 一种和1-硝基蒽醌联产生产二硝基蒽醌的方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE788016A (fr) * | 1971-08-28 | 1973-02-26 | Bayer Ag | Procede de separation de dinitro-anthraquinones pures a partir de melanges de nitration de l'anthraquinone |
| DE2306611C3 (de) * | 1973-02-10 | 1981-10-29 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von 1,5und 1,8-Dinitroanthrachinon |
| DE2334713C3 (de) * | 1973-07-07 | 1980-07-10 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Isolierung von 13-Dinitroanthrachinon |
| DE2346317C3 (de) * | 1973-09-14 | 1980-06-19 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Dinitroanthrachinonen |
| RO64228A (ro) * | 1973-10-13 | 1980-06-15 | Bayer Ag,De | Procedeu de separare a 1,5-dinitroantrachinonei si 1,8-dinitroantrachinonei |
| DE2439280A1 (de) * | 1974-08-16 | 1976-02-26 | Bayer Ag | Verfahren zur herstellung von 1,5dinitroanthrachinon und 1,8-dinitroanthrachinon |
-
1976
- 1976-09-13 JP JP10966976A patent/JPS5334765A/ja active Granted
-
1977
- 1977-08-30 CH CH1053877A patent/CH638486A5/de not_active IP Right Cessation
- 1977-09-07 US US05/831,223 patent/US4158009A/en not_active Expired - Lifetime
- 1977-09-08 DE DE19772740403 patent/DE2740403A1/de active Granted
- 1977-09-08 GB GB37621/77A patent/GB1564054A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US4158009A (en) | 1979-06-12 |
| CH638486A5 (de) | 1983-09-30 |
| GB1564054A (en) | 1980-04-02 |
| JPS5334765A (en) | 1978-03-31 |
| DE2740403A1 (de) | 1978-03-16 |
| JPS5539535B2 (en, 2012) | 1980-10-13 |
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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 | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: MITSUBISHI KASEI CORP., TOKIO/TOKYO, JP |
|
| 8328 | Change in the person/name/address of the agent |
Free format text: STOLBERG-WERNIGERODE, GRAF ZU, U., DIPL.-CHEM. DR.RER.NAT. SUCHANTKE, J., DIPL.-ING., PAT.-ANWAELTE, 2000 HAMBURG |
|
| 8328 | Change in the person/name/address of the agent |
Free format text: STOLBERG-WERNIGERODE, GRAF ZU, U., DIPL.-CHEM. DR.RER.NAT. SUCHANTKE, J., DIPL.-ING., PAT.-ANWAELTE, 2000 HAMBURG |