DE1249866B - Verfahren zur Herstellung von n-Allylnickelhalogemden - Google Patents
Verfahren zur Herstellung von n-AllylnickelhalogemdenInfo
- Publication number
- DE1249866B DE1249866B DENDAT1249866D DE1249866DA DE1249866B DE 1249866 B DE1249866 B DE 1249866B DE NDAT1249866 D DENDAT1249866 D DE NDAT1249866D DE 1249866D A DE1249866D A DE 1249866DA DE 1249866 B DE1249866 B DE 1249866B
- Authority
- DE
- Germany
- Prior art keywords
- allyl
- halides
- nickel
- preparation
- reaction
- 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.)
- Pending
Links
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 title claims description 23
- 229910052759 nickel Inorganic materials 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 12
- -1 allyl halides Chemical class 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 7
- 229910052786 argon Inorganic materials 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 3
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 2
- 229910021585 Nickel(II) bromide Inorganic materials 0.000 description 2
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910002090 carbon oxide Inorganic materials 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- AVMHMVJVHYGDOO-NSCUHMNNSA-N (e)-1-bromobut-2-ene Chemical compound C\C=C\CBr AVMHMVJVHYGDOO-NSCUHMNNSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- OHXAOPZTJOUYKM-UHFFFAOYSA-N 3-Chloro-2-methylpropene Chemical compound CC(=C)CCl OHXAOPZTJOUYKM-UHFFFAOYSA-N 0.000 description 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- HFEHLDPGIKPNKL-UHFFFAOYSA-N allyl iodide Chemical compound ICC=C HFEHLDPGIKPNKL-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- YTKRILODNOEEPX-NSCUHMNNSA-N crotyl chloride Chemical compound C\C=C\CCl YTKRILODNOEEPX-NSCUHMNNSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 150000001983 dialkylethers Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 208000001848 dysentery Diseases 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000006713 insertion reaction Methods 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010414 supernatant solution Substances 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
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/04—Nickel compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEST025041 | 1966-02-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1249866B true DE1249866B (de) | 1967-09-14 |
Family
ID=7460381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT1249866D Pending DE1249866B (de) | 1966-02-26 | Verfahren zur Herstellung von n-Allylnickelhalogemden |
Country Status (7)
| Country | Link |
|---|---|
| BE (1) | BE694637A (el) |
| CH (1) | CH507309A (el) |
| DE (1) | DE1249866B (el) |
| FR (1) | FR1512731A (el) |
| GB (1) | GB1118075A (el) |
| NL (1) | NL6702916A (el) |
| SE (1) | SE321928B (el) |
-
0
- DE DENDAT1249866D patent/DE1249866B/de active Pending
-
1967
- 1967-02-16 CH CH231867A patent/CH507309A/de not_active IP Right Cessation
- 1967-02-21 GB GB817867A patent/GB1118075A/en not_active Expired
- 1967-02-23 SE SE251867A patent/SE321928B/xx unknown
- 1967-02-24 BE BE694637D patent/BE694637A/xx unknown
- 1967-02-24 NL NL6702916A patent/NL6702916A/xx unknown
- 1967-02-24 FR FR96525A patent/FR1512731A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1118075A (en) | 1968-06-26 |
| BE694637A (el) | 1967-08-24 |
| CH507309A (de) | 1971-05-15 |
| FR1512731A (fr) | 1968-02-09 |
| NL6702916A (el) | 1967-08-28 |
| SE321928B (el) | 1970-03-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Arnold et al. | Preparation, spectroscopic properties, and reactivity of trans-hydridoaryl and trans-hydridomethyl complexes of platinum (II) | |
| DE925348C (de) | Verfahren zur Herstellung von Komplexverbindungen aus Aluminiumkohlenwasserstoffen und Alkalifluoriden | |
| DE1254151B (de) | Verfahren zur Herstellung von Organomagnesiumverbindungen | |
| EP0051859A1 (de) | Verfahren zur Herstellung von Ethanol aus Methanol | |
| EP3587430B1 (de) | Herstellung von trialkylpnictogen | |
| DE1249866B (de) | Verfahren zur Herstellung von n-Allylnickelhalogemden | |
| EP0084833B1 (de) | Verfahren zur Herstellung von Ethanol und n-Propanol aus Methanol und Synthesegas | |
| DE2030575A1 (de) | Verfahren zur Hydroformylierung von Olefinen | |
| DE2114769B2 (de) | Verfahren zur Herstellung eines Katalysators für die Ammoniaksynthese | |
| DE2039125C3 (de) | Verfahren zur Herstellung optisch aktiver Kohlenwasserstoffe aus optisch inaktiven Kohlenwasserstoffen unter C-C-Verknuepfung mit Hilfe optisch aktive Zentren enthaltender Katalysatoren | |
| EP0053792B1 (de) | Verfahren zur Herstellung von Ethanol und n-Propanol aus Methanol | |
| DE1060399B (de) | Verfahren zur Herstellung von metallorganischen Verbindungen des Nickels | |
| DE956956C (de) | Verfahren zur Herstellung komplexer Aluminium-Alkalimetall-Alkyle | |
| AT262321B (de) | Verfahren zur Herstellung von π-Allylnickelhalogeniden | |
| DE2310808C2 (de) | Verfahren zur Herstellung von Propionsäure und/oder Propionsäureanhydrid | |
| DE1154476B (de) | Verfahren zur Herstellung von Aluminiumverbindungen des Acetylens | |
| DE2406554A1 (de) | Metathesekatalysatoren, ihre herstellung und verwendung | |
| DE1945303A1 (de) | Verfahren zur gleichzeitigen Herstellung von Alkalialkoholaten und loeslichen beta-Diketonkomplexverbindungen des 3-wertigen Titans | |
| DE69514418T2 (de) | Platinkomplex und diese enthaltende Arzneimittel für die Behandlung von bösartigen Tumoren | |
| DE1061323B (de) | Verfahren zur Herstellung von neuen Titan und Aluminium enthaltenden organischen Komplexverbindungen | |
| DE68902175T2 (de) | Herstellungsverfahren von methylacetat aus methylformiat. | |
| DE2450826A1 (de) | Verfahren zur herstellung von uraniv-chelatverbindungen und thoriumchelatverbindungen | |
| DE1194417B (de) | Verfahren zur Herstellung von pi-Allyl-nickelhalogeniden | |
| DE2221253A1 (de) | Verfahren zur disproportionierung von diallylaminen | |
| DE1767570C (de) | Verfahren zur Herstellung des Tn meren von Ruthemumtetracarbonyl |