CH626374A5 - - Google Patents
Download PDFInfo
- Publication number
- CH626374A5 CH626374A5 CH826475A CH826475A CH626374A5 CH 626374 A5 CH626374 A5 CH 626374A5 CH 826475 A CH826475 A CH 826475A CH 826475 A CH826475 A CH 826475A CH 626374 A5 CH626374 A5 CH 626374A5
- Authority
- CH
- Switzerland
- Prior art keywords
- reaction
- solution
- carried out
- process according
- alkyl
- Prior art date
Links
- 238000009835 boiling Methods 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- -1 amino, hydroxyl Chemical group 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 150000003141 primary amines Chemical class 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 239000007810 chemical reaction solvent Substances 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 239000002879 Lewis base Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 150000007527 lewis bases Chemical class 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 229910000086 alane Inorganic materials 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 22
- 239000000047 product Substances 0.000 description 13
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 7
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 238000004949 mass spectrometry Methods 0.000 description 4
- 230000002035 prolonged effect Effects 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 239000002198 insoluble material Substances 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910010084 LiAlH4 Inorganic materials 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 229910020828 NaAlH4 Inorganic materials 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 150000001793 charged compounds Chemical class 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 238000003760 magnetic stirring Methods 0.000 description 2
- 238000001819 mass spectrum Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 229910010062 TiCl3 Inorganic materials 0.000 description 1
- 229910003074 TiCl4 Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 1
- VJBCNMFKFZIXHC-UHFFFAOYSA-N azanium;2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)quinoline-3-carboxylate Chemical compound N.N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O VJBCNMFKFZIXHC-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- MPOOBUXJJDKJOG-UHFFFAOYSA-M lithium;chloride;hydrochloride Chemical compound [Li+].Cl.[Cl-] MPOOBUXJJDKJOG-UHFFFAOYSA-M 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT24663/74A IT1019678B (it) | 1974-07-01 | 1974-07-01 | N-6-alchil-iminoalani-oligomerici e processo per la loro preparazione |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH626374A5 true CH626374A5 (xx) | 1981-11-13 |
Family
ID=11214306
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH826475A CH626374A5 (xx) | 1974-07-01 | 1975-06-25 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4064153A (xx) |
| JP (1) | JPS5123207A (xx) |
| BE (1) | BE830814A (xx) |
| CA (1) | CA1047515A (xx) |
| CH (1) | CH626374A5 (xx) |
| CS (1) | CS199593B2 (xx) |
| DD (1) | DD123095A5 (xx) |
| DK (1) | DK147021C (xx) |
| FR (1) | FR2277091A1 (xx) |
| GB (1) | GB1508045A (xx) |
| HU (2) | HU176876B (xx) |
| IL (1) | IL47775A (xx) |
| IT (1) | IT1019678B (xx) |
| LU (1) | LU72858A1 (xx) |
| NL (1) | NL172856C (xx) |
| NO (1) | NO752293L (xx) |
| SE (1) | SE432936B (xx) |
| SU (1) | SU637088A3 (xx) |
| YU (2) | YU39469B (xx) |
| ZA (1) | ZA754121B (xx) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4179459A (en) * | 1976-10-28 | 1979-12-18 | Anic S.P.A. | Process for the synthesis of mixed polyimino derivatives of aluminium and alkaline earth metals |
| IT1095573B (it) * | 1978-04-12 | 1985-08-10 | Snam Progetti | Derivati imminici oligomerici dell'idruro di alluminio e processi per la loro preparazione |
| US4325885A (en) * | 1978-04-12 | 1982-04-20 | Anic S.P.A. | Method for preparation of oligomeric iminic derivatives of aluminum |
| US4665207A (en) * | 1985-10-02 | 1987-05-12 | Ethyl Corporation | Preparation of amine alane complexes |
| US4687657A (en) * | 1986-06-09 | 1987-08-18 | Celanese Corporation | Fabrication of SiC - AlN alloys |
| US4748260A (en) * | 1986-12-22 | 1988-05-31 | Ethyl Corporation | Preparation of amine alanes |
| CA2045002A1 (en) * | 1990-10-09 | 1992-04-10 | James A. Jensen | Polymer precursors for aluminum nitride |
| US5457173A (en) * | 1990-10-09 | 1995-10-10 | Lanxide Technology Company, Lp | Polymer precursors for aluminum nitride |
| US5455322A (en) * | 1992-06-12 | 1995-10-03 | Lanxide Technology Company, Lp | Aluminum nitride from inorganic polymers |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3311604A (en) * | 1961-02-04 | 1967-03-28 | Snam Spa | Process for polymerizing isoprene with a catalyst consisting of titanium tetrachloride and an aluminum hydride |
| NL130130C (xx) * | 1961-07-17 | |||
| US3505246A (en) * | 1962-05-28 | 1970-04-07 | Thiokol Chemical Corp | Nitrogen aluminum hydride polymers and method of making the same |
| DE2110195C3 (de) * | 1970-03-11 | 1975-07-31 | Snam Progetti S.P.A., Mailand (Italien) | Aluminiumverbindung, Verfahren zu ihrer Herstellung und ihre Verwendung bei der Polymerisation von Olefinen, konjugierten oder nicht-konjugierten Dienen oder Gemischen davon |
-
1974
- 1974-07-01 IT IT24663/74A patent/IT1019678B/it active
-
1975
- 1975-06-19 GB GB26197/75A patent/GB1508045A/en not_active Expired
- 1975-06-25 NO NO752293A patent/NO752293L/no unknown
- 1975-06-25 CH CH826475A patent/CH626374A5/it not_active IP Right Cessation
- 1975-06-26 CS CS754545A patent/CS199593B2/cs unknown
- 1975-06-26 FR FR7520161A patent/FR2277091A1/fr active Granted
- 1975-06-27 ZA ZA00754121A patent/ZA754121B/xx unknown
- 1975-06-30 HU HU75SA3109A patent/HU176876B/hu unknown
- 1975-06-30 LU LU72858A patent/LU72858A1/xx unknown
- 1975-06-30 HU HU75SA00002814A patent/HU173010B/hu unknown
- 1975-06-30 YU YU1674/75A patent/YU39469B/xx unknown
- 1975-06-30 CA CA230,436A patent/CA1047515A/en not_active Expired
- 1975-06-30 BE BE157823A patent/BE830814A/xx not_active IP Right Cessation
- 1975-06-30 DK DK295675A patent/DK147021C/da not_active IP Right Cessation
- 1975-06-30 JP JP50080151A patent/JPS5123207A/ja active Pending
- 1975-07-01 SE SE7507565A patent/SE432936B/xx unknown
- 1975-07-01 NL NLAANVRAGE7507845,A patent/NL172856C/xx not_active IP Right Cessation
- 1975-07-01 DD DD187013A patent/DD123095A5/xx unknown
- 1975-07-01 US US05/592,248 patent/US4064153A/en not_active Expired - Lifetime
- 1975-07-01 SU SU752151503A patent/SU637088A3/ru active
- 1975-07-23 IL IL47775A patent/IL47775A/xx unknown
-
1981
- 1981-12-18 YU YU03007/81A patent/YU300781A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK147021C (da) | 1984-08-27 |
| DK295675A (da) | 1976-01-02 |
| NL172856B (nl) | 1983-06-01 |
| YU39469B (en) | 1984-12-31 |
| SE432936B (sv) | 1984-04-30 |
| LU72858A1 (xx) | 1975-10-08 |
| IT1019678B (it) | 1977-11-30 |
| YU300781A (en) | 1983-06-30 |
| NL172856C (nl) | 1983-11-01 |
| CS199593B2 (en) | 1980-07-31 |
| SE7507565L (sv) | 1976-01-02 |
| CA1047515A (en) | 1979-01-30 |
| BE830814A (fr) | 1975-10-16 |
| DK147021B (da) | 1984-03-19 |
| ZA754121B (en) | 1976-07-28 |
| HU173010B (hu) | 1979-01-28 |
| FR2277091B1 (xx) | 1977-07-08 |
| DD123095A5 (xx) | 1976-11-20 |
| AU8236975A (en) | 1977-01-06 |
| YU167475A (en) | 1982-05-31 |
| HU176876B (en) | 1981-05-28 |
| DE2529367B2 (de) | 1976-12-16 |
| SU637088A3 (ru) | 1978-12-05 |
| IL47775A0 (en) | 1975-10-15 |
| US4064153A (en) | 1977-12-20 |
| NO752293L (xx) | 1976-01-05 |
| DE2529367A1 (de) | 1976-01-29 |
| JPS5123207A (en) | 1976-02-24 |
| IL47775A (en) | 1979-05-31 |
| GB1508045A (en) | 1978-04-19 |
| NL7507845A (nl) | 1976-01-05 |
| FR2277091A1 (fr) | 1976-01-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100346257B1 (ko) | 유기금속유도체와그제조방법 | |
| CH626374A5 (xx) | ||
| US3812122A (en) | Process for making oxyalkylated polyamino-1,3,5-triazines | |
| SU679144A3 (ru) | Способ получени олигомерных производных гидрида алюмини | |
| Lorberth | Mercury—nitrogen compounds: II. N-(methylmercury) tris (dimethylamino) phosphine imide, MeHgNP (NMe2) 3 | |
| US2757117A (en) | N, n', n''-hexaalkylphosphorohalogenidotriamidothioic acid esters | |
| US3050361A (en) | Decaborane salts and their preparation | |
| Legzdins et al. | Organometallic amido nitrosyl complexes of molybdenum and tungsten | |
| US3373193A (en) | Dimeric halophospha (iii)-carboranes and their production | |
| US3032589A (en) | Method of preparing organophosphorus oxides | |
| US2917543A (en) | Process of producing substituted borazoles | |
| US2437798A (en) | New secondary organic phosphorus halides and processes for making the same | |
| Chadha et al. | Preparation and crystal structures of tetrakis (O, O'-dimethyl dithiophosphato) germanium and bis [(. mu.-sulfido) bis (O, O'-dimethyl dithiophosphato)] digermanium, an unusual sulfur-bridged binuclear compound | |
| US3450728A (en) | Process for the production of complexes of transition metals with cyclooctatetraene | |
| US2969390A (en) | Tris (substituted carbamoyl) phosphines and the preparation thereof | |
| US3048631A (en) | Novel phosphonitrilic isothiocyanate derivatives | |
| US3869509A (en) | N-alkyl-N(trihalomethylthio)-sulfamic acid chloride | |
| US3489812A (en) | Method of preparing bis-(diethyl sulfide)-decaborane | |
| US3057895A (en) | Nitrogenous organometallic compounds | |
| Tarassoli et al. | Studies of the synthesis and thermolysis of tris [tris (amino) phosphine] molybdenum tricarbonyls: synthesis of fac-[(iso-PrNH) 3P] 3Mo (CO) 3 | |
| DE2529367C3 (de) | Verfahren zur Herstellung von oligomeren N-Alkyliminoalanen | |
| Dozzi et al. | The chemistry and stereochemistry of poly (N-alkyliminoalanes). XVII. The syntheses of poly (N-alkyliminoalanes) from dimethylamino-or methoxy-propylamines | |
| US3151145A (en) | Methods for preparing zeta-alkyl-omiron-aryl-thiolcarbonates | |
| Zimmermann et al. | Tetrapodal pentadentate Ligands with NS4 and NP4 donor sets: An elusive tetrathiol, and a sterically encumbered tetraphosphane | |
| Brown et al. | A new methylaminoborane polymer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |