DE2708914C2 - Verfahren und Vorrichtung zur Herstellung von Hydrazobenzol - Google Patents
Verfahren und Vorrichtung zur Herstellung von HydrazobenzolInfo
- Publication number
- DE2708914C2 DE2708914C2 DE19772708914 DE2708914A DE2708914C2 DE 2708914 C2 DE2708914 C2 DE 2708914C2 DE 19772708914 DE19772708914 DE 19772708914 DE 2708914 A DE2708914 A DE 2708914A DE 2708914 C2 DE2708914 C2 DE 2708914C2
- Authority
- DE
- Germany
- Prior art keywords
- hydrazobenzene
- hydrogen
- reactor
- reaction
- nitrobenzene
- 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
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 title claims description 32
- 238000000034 method Methods 0.000 title claims description 17
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims description 50
- 239000001257 hydrogen Substances 0.000 claims description 32
- 229910052739 hydrogen Inorganic materials 0.000 claims description 32
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 29
- 238000006243 chemical reaction Methods 0.000 claims description 22
- 238000005984 hydrogenation reaction Methods 0.000 claims description 22
- 239000011541 reaction mixture Substances 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 9
- 239000007789 gas Substances 0.000 claims description 8
- 239000012298 atmosphere Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 230000001476 alcoholic effect Effects 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 230000003197 catalytic effect Effects 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 32
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000003054 catalyst Substances 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000012065 filter cake Substances 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 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 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- MJGFBOZCAJSGQW-UHFFFAOYSA-N mercury sodium Chemical compound [Na].[Hg] MJGFBOZCAJSGQW-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- ZNCXUFVDFVBRDO-UHFFFAOYSA-N pyridine;sulfuric acid Chemical compound [H+].[O-]S([O-])(=O)=O.C1=CC=[NH+]C=C1 ZNCXUFVDFVBRDO-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910001023 sodium amalgam Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772708914 DE2708914C2 (de) | 1977-03-02 | 1977-03-02 | Verfahren und Vorrichtung zur Herstellung von Hydrazobenzol |
| GB3185877A GB1560004A (en) | 1976-08-03 | 1977-07-28 | Process for producing hydrazobenzene |
| HUDI000294 HU178508B (en) | 1976-08-03 | 1977-08-01 | Process and equipment for preparing hydrazobenzene |
| IT5052577A IT1115946B (it) | 1976-08-03 | 1977-08-01 | Procedimento e dispositivo per la produzione di idrazobenzolo |
| JP9291777A JPS5318522A (en) | 1976-08-03 | 1977-08-02 | Method and apparatus for production of hydrazobenzene |
| CH949177A CH629752A5 (en) | 1976-08-03 | 1977-08-02 | Process for preparing hydrazobenzene |
| CS511777A CS204007B2 (en) | 1976-08-03 | 1977-08-02 | Process for preparing hydrazobenzene |
| FR7723808A FR2360563A1 (fr) | 1976-08-03 | 1977-08-02 | Procede pour l'obtention d'hydrazobenzene |
| NL7708542A NL7708542A (nl) | 1976-08-03 | 1977-08-02 | Werkwijze voor het bereiden van hydrazobenzeen. |
| ES461272A ES461272A1 (es) | 1976-08-03 | 1977-08-03 | Procedimiento para la preparacion de hidrazobenceno. |
| ES470767A ES470767A1 (es) | 1976-08-03 | 1978-06-14 | Dispositivo para la preparacion de hidrazobenceno |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772708914 DE2708914C2 (de) | 1977-03-02 | 1977-03-02 | Verfahren und Vorrichtung zur Herstellung von Hydrazobenzol |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2708914A1 DE2708914A1 (de) | 1978-09-07 |
| DE2708914C2 true DE2708914C2 (de) | 1987-05-14 |
Family
ID=6002510
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772708914 Expired DE2708914C2 (de) | 1976-08-03 | 1977-03-02 | Verfahren und Vorrichtung zur Herstellung von Hydrazobenzol |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE2708914C2 (US07993877-20110809-P00003.png) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB599252A (en) * | 1944-01-27 | 1948-03-09 | Standard Oil Dev Co | Improved process for the production of aromatic amines |
| DE1114820B (de) * | 1960-01-15 | 1961-10-12 | Basf Ag | Verfahren zur Herstellung von Anilin |
| US3260750A (en) * | 1963-10-14 | 1966-07-12 | Upjohn Co | Process for preparing hydrazobenzenes |
| FR1404710A (fr) * | 1964-06-12 | 1965-07-02 | Basf Ag | Procédé pour la produiction de catalyseurs ou de supports de catalyseurs sous formede billes creuses |
| CH490317A (de) * | 1967-12-01 | 1970-05-15 | Lonza Ag | Verfahren zur Durchführung der katalytischen Gasphasenhydrierung von organischen Nitroverbindungen zu den entsprechenden Aminen |
-
1977
- 1977-03-02 DE DE19772708914 patent/DE2708914C2/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2708914A1 (de) | 1978-09-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH398564A (de) | Verfahren zur Herstellung von Cyclohexanon | |
| EP0007972B1 (de) | Verfahren zur Herstellung von Dichlorhydrazobenzolen durch katalytische Hydrierung von Monochlornitrobenzolen | |
| EP0004919B1 (de) | Verfahren zur Herstellung von N,N,N',N'-Tetraacetyl-ethylendiamin | |
| DE3214247C2 (US07993877-20110809-P00003.png) | ||
| DE2708914C2 (de) | Verfahren und Vorrichtung zur Herstellung von Hydrazobenzol | |
| DE1200281B (de) | Verfahren zur Herstellung von Acetessigsaeureestern | |
| DE3443385A1 (de) | Verfahren zur herstellung eines 4-alkoxyanilins | |
| EP0648748B1 (de) | Verfahren zur Herstellung von 5-Acetoacetylaminobenzimidazolon-2 | |
| EP0453949B1 (de) | Verfahren zur Herstellung von Alkyltetrahydroanthrahydrochinonlösungen und ihre Verwendung als Arbeitslösung bei der Wasserstoffperoxid-Herstellung nach dem Anthrachinonverfahren | |
| EP0089417B1 (de) | Verfahren zur Herstellung von Phthalid | |
| EP0225850A1 (de) | Verfahren zur Herstellung von 1-(2-Hydroxyethyl)-2,2,6,6-tetramethyl-4-hydroxy-piperidin | |
| EP0190424B1 (de) | Verfahren zur Herstellung reiner Dialkylsuccinate | |
| CH629752A5 (en) | Process for preparing hydrazobenzene | |
| DE2634861C2 (de) | Verfahren zur Herstellung von Hydrazobenzol | |
| DE2634862C2 (de) | Verfahren zur Herstellung von Hydrazobenzol | |
| EP0950653B1 (de) | Verfahren zur Herstellung von Kaliummonoethylmalonat | |
| DE2825347C2 (de) | Verfahren zur Herstellung von p-Hydroxymethylbenzoesäurealkylestern | |
| EP0444266B1 (de) | Verfahren zur Herstellung von 2,4,5-Triamino-6-hydroxypyrimidin durch katalytische Hydrierung von 2,4-Diamino-6-hydroxy-5-nitrosopyrimidin | |
| EP0054809B1 (de) | Verfahren zur Herstellung von 5-Amino-2,4-dimethyl-acetanilid | |
| DE2614294B2 (de) | Verfahren zur Herstellung von Phthalid | |
| AT209885B (de) | Verfahren und Vorrichtung zur Herstellung von Diacetonalkohol | |
| DE1144267B (de) | Verfahren zur Herstellung von Cyclohexanon | |
| DE2218316B2 (de) | Verfahren zur Herstellung von Anthrachinon | |
| DE1298977B (de) | Verfahren zur Gewinnung von Adipinsaeure | |
| DE2847625A1 (de) | Verfahren zur herstellung eines oxazols |
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: HUELS TROISDORF AG, 5210 TROISDORF, DE |
|
| 8339 | Ceased/non-payment of the annual fee |