CA1087633A - Process for the production of polyaryl amines containing methylene bridges - Google Patents
Process for the production of polyaryl amines containing methylene bridgesInfo
- Publication number
- CA1087633A CA1087633A CA264,973A CA264973A CA1087633A CA 1087633 A CA1087633 A CA 1087633A CA 264973 A CA264973 A CA 264973A CA 1087633 A CA1087633 A CA 1087633A
- Authority
- CA
- Canada
- Prior art keywords
- arylamine
- acid
- aniline
- salt
- amine
- 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
- 238000000034 method Methods 0.000 title claims abstract description 48
- 150000001412 amines Chemical class 0.000 title abstract description 22
- 238000004519 manufacturing process Methods 0.000 title abstract description 5
- 150000004982 aromatic amines Chemical class 0.000 claims abstract description 77
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
- 150000003839 salts Chemical class 0.000 claims abstract description 28
- 239000002253 acid Substances 0.000 claims abstract description 26
- 239000000203 mixture Substances 0.000 claims abstract description 26
- 239000003054 catalyst Substances 0.000 claims abstract description 12
- 239000002904 solvent Substances 0.000 claims abstract description 10
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 82
- 239000000243 solution Substances 0.000 claims description 23
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 18
- 239000008346 aqueous phase Substances 0.000 claims description 12
- 238000009833 condensation Methods 0.000 claims description 12
- 230000005494 condensation Effects 0.000 claims description 12
- 239000012074 organic phase Substances 0.000 claims description 10
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 8
- -1 poly-amine salt Chemical class 0.000 claims description 8
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 claims description 6
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 claims description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 238000010790 dilution Methods 0.000 claims description 4
- 239000012895 dilution Substances 0.000 claims description 4
- 238000011084 recovery Methods 0.000 claims description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 239000011260 aqueous acid Substances 0.000 claims 1
- 238000007865 diluting Methods 0.000 claims 1
- 239000012266 salt solution Substances 0.000 abstract description 14
- 239000007864 aqueous solution Substances 0.000 abstract description 9
- 150000007513 acids Chemical class 0.000 abstract description 8
- 238000007796 conventional method Methods 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229960004279 formaldehyde Drugs 0.000 abstract 1
- 235000019256 formaldehyde Nutrition 0.000 abstract 1
- 229920000768 polyamine Polymers 0.000 description 22
- 239000012071 phase Substances 0.000 description 12
- 238000007792 addition Methods 0.000 description 9
- 238000009434 installation Methods 0.000 description 9
- 238000000605 extraction Methods 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 239000003377 acid catalyst Substances 0.000 description 7
- MMCPOSDMTGQNKG-UHFFFAOYSA-N anilinium chloride Chemical compound Cl.NC1=CC=CC=C1 MMCPOSDMTGQNKG-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- GGFOZRQCNXQCLO-UHFFFAOYSA-N aniline;methanesulfonic acid Chemical compound CS(O)(=O)=O.NC1=CC=CC=C1 GGFOZRQCNXQCLO-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 230000008707 rearrangement Effects 0.000 description 3
- UFFBMTHBGFGIHF-UHFFFAOYSA-N 2,6-dimethylaniline Chemical compound CC1=CC=CC(C)=C1N UFFBMTHBGFGIHF-UHFFFAOYSA-N 0.000 description 2
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- WKBALTUBRZPIPZ-UHFFFAOYSA-N 2,6-di(propan-2-yl)aniline Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N WKBALTUBRZPIPZ-UHFFFAOYSA-N 0.000 description 1
- FOYHNROGBXVLLX-UHFFFAOYSA-N 2,6-diethylaniline Chemical compound CCC1=CC=CC(CC)=C1N FOYHNROGBXVLLX-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical class C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 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
- C07C209/68—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
- C07C209/78—Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton from carbonyl compounds, e.g. from formaldehyde, and amines having amino groups bound to carbon atoms of six-membered aromatic rings, with formation of methylene-diarylamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/06—Amines
- C08G12/08—Amines aromatic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH14618 | 1975-11-11 | ||
| CH1461875 | 1975-11-11 | ||
| CH5854 | 1976-05-05 | ||
| CH585476 | 1976-05-05 | ||
| CH1004976 | 1976-08-04 | ||
| CH10049 | 1976-08-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1087633A true CA1087633A (en) | 1980-10-14 |
Family
ID=27175350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA264,973A Expired CA1087633A (en) | 1975-11-11 | 1976-11-05 | Process for the production of polyaryl amines containing methylene bridges |
Country Status (22)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE848T1 (de) * | 1978-09-12 | 1982-04-15 | Gebrueder Sulzer Aktiengesellschaft | Verfahren zur herstellung von methylenbruecken aufweisenden polyarylaminen. |
| EP2062869A1 (en) | 2007-09-19 | 2009-05-27 | Huntsman International Llc | Process for the production of di-and polyamines of the diphenylmethane series |
| EP2039676A1 (en) | 2007-09-19 | 2009-03-25 | Huntsman International Llc | Process for the production of di-and polyamines of the diphenylmethane series |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3367969A (en) * | 1965-03-08 | 1968-02-06 | Du Pont | Process for the preparation of 4, 4'-methylenedianiline |
| GB1287141A (en) * | 1969-01-01 | 1972-08-31 | Ici Ltd | Manufacture of methylene-bridged polyarylamines |
| DE2227110C3 (de) * | 1972-06-03 | 1984-08-23 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyaminen |
| DE2238378C3 (de) * | 1972-08-04 | 1975-01-09 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Perlnonfarbstoffe und Verfahren zu Ihrer Herstellung |
| DE2238920C3 (de) * | 1972-08-08 | 1984-09-27 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyaminen |
| DE2343658C2 (de) * | 1973-08-30 | 1982-06-03 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyaminen |
| DE2356828C2 (de) * | 1973-11-14 | 1982-10-21 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyaminen und ihre Verwendung als Ausgangsmaterial zur Herstellung von Polyisocyanaten |
| DE2500573A1 (de) * | 1975-01-09 | 1976-07-15 | Bayer Ag | Verfahren zur herstellung von polyaminen |
-
1976
- 1976-10-28 DE DE2648982A patent/DE2648982C2/de not_active Expired
- 1976-10-29 IE IE2421/76A patent/IE44544B1/en unknown
- 1976-11-05 PT PT65803A patent/PT65803B/pt unknown
- 1976-11-05 YU YU02717/76A patent/YU271776A/xx unknown
- 1976-11-05 CA CA264,973A patent/CA1087633A/en not_active Expired
- 1976-11-05 IL IL50857A patent/IL50857A/xx unknown
- 1976-11-06 RO RO7688358A patent/RO79103A/ro unknown
- 1976-11-06 GR GR52122A patent/GR60355B/el unknown
- 1976-11-09 LU LU76153A patent/LU76153A1/xx unknown
- 1976-11-09 SE SE7612478A patent/SE421533B/xx unknown
- 1976-11-09 PL PL1976193576A patent/PL104368B1/pl unknown
- 1976-11-09 DD DD7600195684A patent/DD128184A5/xx unknown
- 1976-11-10 BR BR7607527A patent/BR7607527A/pt unknown
- 1976-11-10 ES ES453159A patent/ES453159A1/es not_active Expired
- 1976-11-10 TR TR19975A patent/TR19975A/xx unknown
- 1976-11-10 MX MX166949A patent/MX148753A/es unknown
- 1976-11-10 FR FR7634029A patent/FR2331575A1/fr active Granted
- 1976-11-10 GB GB46742/76A patent/GB1567638A/en not_active Expired
- 1976-11-11 AT AT0836676A patent/ATA836676A/de not_active Application Discontinuation
- 1976-11-11 NL NL7612539A patent/NL7612539A/xx not_active Application Discontinuation
- 1976-11-11 JP JP51136170A patent/JPS5260895A/ja active Pending
- 1976-11-11 DK DK508476A patent/DK508476A/da not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| GB1567638A (en) | 1980-05-21 |
| IE44544B1 (en) | 1981-12-30 |
| PL104368B1 (pl) | 1979-08-31 |
| NL7612539A (nl) | 1977-05-13 |
| ATA836676A (de) | 1982-08-15 |
| GR60355B (en) | 1978-05-18 |
| FR2331575A1 (fr) | 1977-06-10 |
| MX148753A (es) | 1983-06-14 |
| LU76153A1 (enrdf_load_stackoverflow) | 1977-05-18 |
| YU271776A (en) | 1982-05-31 |
| DK508476A (da) | 1977-05-12 |
| SE421533B (sv) | 1982-01-04 |
| PT65803A (en) | 1976-12-01 |
| JPS5260895A (en) | 1977-05-19 |
| RO79103A (ro) | 1982-06-25 |
| IL50857A (en) | 1981-05-20 |
| PT65803B (en) | 1978-05-12 |
| DE2648982C2 (de) | 1985-07-11 |
| DE2648982A1 (de) | 1977-05-26 |
| IL50857A0 (en) | 1977-01-31 |
| FR2331575B1 (enrdf_load_stackoverflow) | 1980-05-09 |
| BR7607527A (pt) | 1977-09-20 |
| SE7612478L (sv) | 1977-05-12 |
| ES453159A1 (es) | 1978-03-01 |
| IE44544L (en) | 1977-05-11 |
| DD128184A5 (de) | 1977-11-02 |
| TR19975A (tr) | 1980-06-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |