DE2521293C3 - Verfahren zur Herstellung von Diphenylamin - Google Patents
Verfahren zur Herstellung von DiphenylaminInfo
- Publication number
- DE2521293C3 DE2521293C3 DE2521293A DE2521293A DE2521293C3 DE 2521293 C3 DE2521293 C3 DE 2521293C3 DE 2521293 A DE2521293 A DE 2521293A DE 2521293 A DE2521293 A DE 2521293A DE 2521293 C3 DE2521293 C3 DE 2521293C3
- Authority
- DE
- Germany
- Prior art keywords
- aniline
- reaction
- diphenylamine
- boron
- weight
- 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
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 title claims description 70
- 238000000034 method Methods 0.000 title claims description 19
- 238000002360 preparation method Methods 0.000 title claims description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 98
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 13
- 229910021529 ammonia Inorganic materials 0.000 claims description 11
- 239000003054 catalyst Substances 0.000 claims description 11
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims description 10
- 229910015900 BF3 Inorganic materials 0.000 claims description 8
- -1 ammonium fluoroborate Chemical compound 0.000 claims description 8
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 7
- 239000004327 boric acid Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 5
- RILZRCJGXSFXNE-UHFFFAOYSA-N 2-[4-(trifluoromethoxy)phenyl]ethanol Chemical compound OCCC1=CC=C(OC(F)(F)F)C=C1 RILZRCJGXSFXNE-UHFFFAOYSA-N 0.000 claims description 3
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims 4
- 238000006243 chemical reaction Methods 0.000 description 29
- 239000011541 reaction mixture Substances 0.000 description 24
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 22
- 230000035484 reaction time Effects 0.000 description 16
- LIQLLTGUOSHGKY-UHFFFAOYSA-N [B].[F] Chemical class [B].[F] LIQLLTGUOSHGKY-UHFFFAOYSA-N 0.000 description 15
- 238000003756 stirring Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- GYCAYSIUPQIJIP-UHFFFAOYSA-N [B].[F].NC1=CC=CC=C1 Chemical compound [B].[F].NC1=CC=CC=C1 GYCAYSIUPQIJIP-UHFFFAOYSA-N 0.000 description 1
- VWKLICCSBFEWSZ-UHFFFAOYSA-N aniline;trifluoroborane Chemical compound FB(F)F.NC1=CC=CC=C1 VWKLICCSBFEWSZ-UHFFFAOYSA-N 0.000 description 1
- HPVJGAZWQLWNKJ-UHFFFAOYSA-N azane;trifluoroborane Chemical compound N.FB(F)F HPVJGAZWQLWNKJ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000001739 density measurement Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/64—Preparation of compounds containing amino groups bound to a carbon skeleton by disproportionation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/08—Halides
- B01J27/12—Fluorides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/30—Complexes comprising metals of Group III (IIIA or IIIB) as the central metal
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Priority Applications (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2521293A DE2521293C3 (de) | 1975-05-13 | 1975-05-13 | Verfahren zur Herstellung von Diphenylamin |
| CH765843A CH608781A5 (en) | 1975-05-13 | 1976-05-10 | Process for the preparation of diphenylamine |
| JP51052876A JPS584706B2 (ja) | 1975-05-13 | 1976-05-11 | ジフエニルアミンの製造方法 |
| IT49411/76A IT1061268B (it) | 1975-05-13 | 1976-05-11 | Procedimento per la produzione di difenilammina |
| LU74916A LU74916A1 (cg-RX-API-DMAC10.html) | 1975-05-13 | 1976-05-11 | |
| GB19349/76A GB1483173A (en) | 1975-05-13 | 1976-05-11 | Process for the preparation of diphenylamine |
| CA252,188A CA1067519A (en) | 1975-05-13 | 1976-05-11 | Process for preparing diphenylamine |
| ES447825A ES447825A1 (es) | 1975-05-13 | 1976-05-12 | Procedimiento para la obtencion de difenilamina. |
| BR7602968A BR7602968A (pt) | 1975-05-13 | 1976-05-12 | Processo para a preparacao de difenilamina |
| ZA762832A ZA762832B (en) | 1975-05-13 | 1976-05-12 | Process for the preparation of diphenylamine |
| NL7605129A NL7605129A (nl) | 1975-05-13 | 1976-05-13 | Werkwijze ter bereiding van difenylamine. |
| FR7614490A FR2310997A1 (fr) | 1975-05-13 | 1976-05-13 | Procede de preparation de la diphenylamine |
| BE2055024A BE841762A (fr) | 1975-05-13 | 1976-05-13 | Procede de preparation de la diphenylamine |
| US05/822,979 US4100195A (en) | 1975-05-13 | 1977-08-08 | Process for preparing diphenylamine in the presence of a boron/fluorine compound and water |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2521293A DE2521293C3 (de) | 1975-05-13 | 1975-05-13 | Verfahren zur Herstellung von Diphenylamin |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2521293A1 DE2521293A1 (de) | 1976-11-18 |
| DE2521293B2 DE2521293B2 (de) | 1979-07-12 |
| DE2521293C3 true DE2521293C3 (de) | 1987-12-03 |
Family
ID=5946450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2521293A Expired DE2521293C3 (de) | 1975-05-13 | 1975-05-13 | Verfahren zur Herstellung von Diphenylamin |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS584706B2 (cg-RX-API-DMAC10.html) |
| BE (1) | BE841762A (cg-RX-API-DMAC10.html) |
| BR (1) | BR7602968A (cg-RX-API-DMAC10.html) |
| CA (1) | CA1067519A (cg-RX-API-DMAC10.html) |
| CH (1) | CH608781A5 (cg-RX-API-DMAC10.html) |
| DE (1) | DE2521293C3 (cg-RX-API-DMAC10.html) |
| ES (1) | ES447825A1 (cg-RX-API-DMAC10.html) |
| FR (1) | FR2310997A1 (cg-RX-API-DMAC10.html) |
| GB (1) | GB1483173A (cg-RX-API-DMAC10.html) |
| IT (1) | IT1061268B (cg-RX-API-DMAC10.html) |
| LU (1) | LU74916A1 (cg-RX-API-DMAC10.html) |
| NL (1) | NL7605129A (cg-RX-API-DMAC10.html) |
| ZA (1) | ZA762832B (cg-RX-API-DMAC10.html) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19756146A1 (de) * | 1997-12-17 | 1999-06-24 | Bayer Ag | Herstellung von N-Phenyl-1-naphthylamin |
| DE19756158A1 (de) * | 1997-12-17 | 1999-06-24 | Bayer Ag | Herstellung von sekundären Diarylaminen |
| DE19756145A1 (de) * | 1997-12-17 | 1999-06-24 | Bayer Ag | Herstellung von N-Phenyl-1-naphthylamin |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE694781C (de) * | 1938-06-15 | 1940-08-07 | I G Farbenindustrie Akt Ges | Verfahren zur Darstellung von Phenolen |
| FR1231215A (fr) * | 1959-04-10 | 1960-09-27 | Cfmc | Nouveau procédé de préparation de la diphénylamine |
| US3071619A (en) * | 1959-06-09 | 1963-01-01 | Goodrich Co B F | Preparation of secondary aryl amines |
-
1975
- 1975-05-13 DE DE2521293A patent/DE2521293C3/de not_active Expired
-
1976
- 1976-05-10 CH CH765843A patent/CH608781A5/xx not_active IP Right Cessation
- 1976-05-11 IT IT49411/76A patent/IT1061268B/it active
- 1976-05-11 GB GB19349/76A patent/GB1483173A/en not_active Expired
- 1976-05-11 CA CA252,188A patent/CA1067519A/en not_active Expired
- 1976-05-11 JP JP51052876A patent/JPS584706B2/ja not_active Expired
- 1976-05-11 LU LU74916A patent/LU74916A1/xx unknown
- 1976-05-12 ZA ZA762832A patent/ZA762832B/xx unknown
- 1976-05-12 BR BR7602968A patent/BR7602968A/pt unknown
- 1976-05-12 ES ES447825A patent/ES447825A1/es not_active Expired
- 1976-05-13 FR FR7614490A patent/FR2310997A1/fr active Granted
- 1976-05-13 NL NL7605129A patent/NL7605129A/xx not_active Application Discontinuation
- 1976-05-13 BE BE2055024A patent/BE841762A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| BE841762A (fr) | 1976-11-16 |
| NL7605129A (nl) | 1976-11-16 |
| BR7602968A (pt) | 1977-05-31 |
| ZA762832B (en) | 1977-04-27 |
| DE2521293A1 (de) | 1976-11-18 |
| JPS51138628A (en) | 1976-11-30 |
| CH608781A5 (en) | 1979-01-31 |
| ES447825A1 (es) | 1977-07-01 |
| GB1483173A (en) | 1977-08-17 |
| IT1061268B (it) | 1983-02-28 |
| FR2310997A1 (fr) | 1976-12-10 |
| CA1067519A (en) | 1979-12-04 |
| FR2310997B1 (cg-RX-API-DMAC10.html) | 1979-08-10 |
| JPS584706B2 (ja) | 1983-01-27 |
| LU74916A1 (cg-RX-API-DMAC10.html) | 1977-02-11 |
| DE2521293B2 (de) | 1979-07-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2850680C2 (cg-RX-API-DMAC10.html) | ||
| DE2151417B2 (de) | Verfahren zur Herstellung von Katalysatoren | |
| DE1284412B (de) | Verfahren zur Herstellung von Telomerisationsprodukten | |
| DE2855504B2 (de) | Verfahren zur Herstellung von Methacrolein | |
| DE2418592C2 (de) | Verfahren zur Herstellung von Thiocarbaminsäureestern | |
| DE2521293C3 (de) | Verfahren zur Herstellung von Diphenylamin | |
| DE3106476A1 (de) | Verfahren zur herstellung von trioxan | |
| DE3007139C2 (de) | Kupferchromit-Katalysator, Verfahren zu seiner Herstellung und seine Verwendung zur Herstellung von Alkoholen aus ungesättigten Aldehyden | |
| DE3432015A1 (de) | Verfahren zur herstellung von aminen | |
| DE2651531C2 (de) | Fluorierte Acylfluoride mit einer Estergruppe und Verfahren zu deren Herstellung | |
| DE3422936C2 (cg-RX-API-DMAC10.html) | ||
| DE2329545C2 (de) | 1,2-Bis-oxazolinyl-(2)-cyclobutane und Verfahren zu ihrer Herstellung | |
| DE2314950C3 (de) | Verfahren zur Herstellung von Hydroxydiphenyl | |
| DE2855845C2 (cg-RX-API-DMAC10.html) | ||
| DE1932937C (de) | Verfahren zur Herstellung von Tnalkenyl isoeyanuraten | |
| DE2332064C2 (de) | Verfahren zur Herstellung von 2-Hydroxy-naphthalin-3-carbonsäure | |
| DE3018562C2 (de) | Verfahren zur Herstellung von Dichlorbuten | |
| DE946710C (de) | Verfahren zur Herstellung von N-disubstituierten Sulfamidsaeurechloriden | |
| DE956046C (de) | Verfahren zur Herstellung von Diphenylamin und kernalkylsubstituierten Diphenylaminen | |
| DE1911207C3 (de) | Verfahren zur Herstellung von Natriumtetrolat | |
| DE820303C (de) | Verfahren zur Herstellung organischer Saeuren sowie deren Ester | |
| DE954238C (de) | Verfahren zur Herstellung von Fluoralkanen durch chemische Reduktion von Dichlordifluormethan | |
| DE2503660A1 (de) | Verfahren zur herstellung von diphenylamin | |
| DE1802420C (de) | Verfahren zur Herstellung von Vanillin durch Isomensieren von Eugenol | |
| AT352097B (de) | Verfahren zur herstellung von cyanformamid aus cyanwasserstoff und sauerstoff |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8281 | Inventor (new situation) |
Free format text: FISCHLER, H.-MICHAEL, DR. BAUER, DIETER, DR. QUAST, HEIN, DR., 4150 KREFELD, DE |
|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |