DE2819980C2 - Verfahren zur Herstellung von 3(4), 8(9)-Bis-(isocyanatomethyl)-tricyclo-[5.2.1.0↑2↑↑,↑↑6↑]decanen - Google Patents
Verfahren zur Herstellung von 3(4), 8(9)-Bis-(isocyanatomethyl)-tricyclo-[5.2.1.0↑2↑↑,↑↑6↑]decanenInfo
- Publication number
- DE2819980C2 DE2819980C2 DE19782819980 DE2819980A DE2819980C2 DE 2819980 C2 DE2819980 C2 DE 2819980C2 DE 19782819980 DE19782819980 DE 19782819980 DE 2819980 A DE2819980 A DE 2819980A DE 2819980 C2 DE2819980 C2 DE 2819980C2
- Authority
- DE
- Germany
- Prior art keywords
- uarr
- phosgene
- phosgenation
- tricyclo
- bis
- 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 description 18
- 238000002360 preparation method Methods 0.000 title claims description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 20
- 150000004985 diamines Chemical class 0.000 claims description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000010409 thin film Substances 0.000 claims description 8
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 6
- 238000006386 neutralization reaction Methods 0.000 claims description 6
- 239000012442 inert solvent Substances 0.000 claims description 3
- 239000001569 carbon dioxide Substances 0.000 claims description 2
- 239000000725 suspension Substances 0.000 description 18
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 10
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 125000005442 diisocyanate group Chemical group 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- -1 amine hydrochloride Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- VWPHTOATEPXMCB-UHFFFAOYSA-N carbamoyl chloride;hydrochloride Chemical compound Cl.NC(Cl)=O VWPHTOATEPXMCB-UHFFFAOYSA-N 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- OCKGFTQIICXDQW-ZEQRLZLVSA-N 5-[(1r)-1-hydroxy-2-[4-[(2r)-2-hydroxy-2-(4-methyl-1-oxo-3h-2-benzofuran-5-yl)ethyl]piperazin-1-yl]ethyl]-4-methyl-3h-2-benzofuran-1-one Chemical compound C1=C2C(=O)OCC2=C(C)C([C@@H](O)CN2CCN(CC2)C[C@H](O)C2=CC=C3C(=O)OCC3=C2C)=C1 OCKGFTQIICXDQW-ZEQRLZLVSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- XGDAKJKCJURQAF-UHFFFAOYSA-N azane;carbamic acid Chemical compound N.N.NC(O)=O XGDAKJKCJURQAF-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000007938 chlorocyclic compounds Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- LIAWOTKNAVAKCX-UHFFFAOYSA-N hydrazine;dihydrochloride Chemical compound Cl.Cl.NN LIAWOTKNAVAKCX-UHFFFAOYSA-N 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009183 running Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782819980 DE2819980C2 (de) | 1978-05-08 | 1978-05-08 | Verfahren zur Herstellung von 3(4), 8(9)-Bis-(isocyanatomethyl)-tricyclo-[5.2.1.0↑2↑↑,↑↑6↑]decanen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782819980 DE2819980C2 (de) | 1978-05-08 | 1978-05-08 | Verfahren zur Herstellung von 3(4), 8(9)-Bis-(isocyanatomethyl)-tricyclo-[5.2.1.0↑2↑↑,↑↑6↑]decanen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2819980A1 DE2819980A1 (de) | 1979-11-22 |
| DE2819980C2 true DE2819980C2 (de) | 1987-03-26 |
Family
ID=6038834
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19782819980 Expired DE2819980C2 (de) | 1978-05-08 | 1978-05-08 | Verfahren zur Herstellung von 3(4), 8(9)-Bis-(isocyanatomethyl)-tricyclo-[5.2.1.0↑2↑↑,↑↑6↑]decanen |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE2819980C2 (en17) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102712499B1 (ko) | 2018-06-15 | 2024-10-02 | 에스케이케미칼 주식회사 | 3(4),8(9)-비스포밀트리사이클로[5.2.1.0^2,6]데칸의 제조방법 |
| EP3808728A4 (en) | 2018-06-15 | 2022-03-30 | SK Chemicals Co., Ltd. | METHOD FOR THE PREPARATION OF 3(4),8(9)-BISFORMYLTRICYCLO[5.2.1.0²,6]DECANE |
-
1978
- 1978-05-08 DE DE19782819980 patent/DE2819980C2/de not_active Expired
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2819980A1 (de) | 1979-11-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0749958B1 (de) | Verfahren zur Herstellung von Triisocyanaten | |
| DE69011358T2 (de) | Verfahren zur Herstellung von Xylylendiisocyanat. | |
| DE1202785B (de) | Verfahren zur Herstellung von 1-Isocyanato-3-(isocyanatomethyl)-3, 5, 5-trimethylcyclohexan | |
| DE19804915A1 (de) | Verfahren zur Herstellung von Methylendi(phenylamin) und Methylendi(phenylisocyanat) | |
| EP0792263A1 (de) | Verfahren zur herstellung von isocyanaten | |
| EP0150769B1 (de) | Verfahren zur Herstellung von Polyisocyanaten mit Biuretstruktur | |
| EP1078918A1 (de) | Verfahren zur Herstellung von Diisocyanaten | |
| EP2028179A1 (de) | Herstellung von isocyanaten mit niedrigen chlorgehalten | |
| DE19827086A1 (de) | Verfahren zur Aufarbeitung von Destillationsrückständen aus der Synthese von Toluylendiisocyanat | |
| EP0106138B1 (de) | Verfahren zur kontinuierlichen Heissphosgenierung von Aminen | |
| DE69107212T2 (de) | Verfahren zur Herstellung von polymerischen Methylen-dyphenylen-diisocyanaten mit verminderter Farbe und Chloridgehalt. | |
| EP0083442B1 (de) | Verfahren zur Herstellung von 2,4,6-Trichloranilin | |
| EP0071080A2 (de) | Verfahren zur Herstellung von Polyisocyanaten | |
| DE2005309C3 (de) | Verfahren zur Herstellung von 1,3-Cyclohexylendiisocyanaten | |
| DE2819980C2 (de) | Verfahren zur Herstellung von 3(4), 8(9)-Bis-(isocyanatomethyl)-tricyclo-[5.2.1.0↑2↑↑,↑↑6↑]decanen | |
| DE1593588C3 (de) | Verfahren zur Herstellung von m- und p-Xylylendiisocyanat | |
| EP0104551B1 (de) | Gegebenenfalls Isomerengemische darstellende cycloaliphatische Diisocyanate, ein Verfahren zu ihrer Herstellung, sowie ihre Verwendung als Ausgangsmaterialien bei der Herstellung von Polyurethankunststoffen | |
| DE1123662B (de) | Verfahren zur Herstellung von Alkylbenzoldiisocyanaten | |
| EP0764633A2 (de) | Verfahren zur Herstellung von Etherisocyanaten | |
| DE2747524A1 (de) | Verfahren und vorrichtung zur kontinuierlichen herstellung aromatischer isocyanate | |
| DE1154092B (de) | Verfahren zur Herstellung von AEthergruppen enthaltenden Polyisocyanaten | |
| DE926845C (de) | Verfahren zur Herstellung von p-Phenylendiisocyanat | |
| DE2830243C2 (en17) | ||
| DE19521800C2 (de) | Verfahren zur Herstellung von Isocyanaten | |
| EP0010672B1 (de) | Verfahren zur Herstellung von 1-Fluor-1,2-dichloräthylen durch Dehydrochlorierung von 1-Fluor-1,1,2-trichloräthan |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8127 | New person/name/address of the applicant |
Owner name: HUELS AG, 4370 MARL, DE |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |