DE245180C - - Google Patents
Info
- Publication number
- DE245180C DE245180C DENDAT245180D DE245180DA DE245180C DE 245180 C DE245180 C DE 245180C DE NDAT245180 D DENDAT245180 D DE NDAT245180D DE 245180D A DE245180D A DE 245180DA DE 245180 C DE245180 C DE 245180C
- Authority
- DE
- Germany
- Prior art keywords
- reaction
- butadiene
- vinyl
- magnesium
- preparation
- 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.)
- Active
Links
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 12
- -1 vinyl hydrocarbons Chemical class 0.000 claims description 10
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 1
- PNLQPWWBHXMFCA-UHFFFAOYSA-N 2-chloroprop-1-ene Chemical group CC(Cl)=C PNLQPWWBHXMFCA-UHFFFAOYSA-N 0.000 description 1
- 241000341924 Buthus paris Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 150000001722 carbon compounds Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N dimethyl-butadiene Natural products CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N penta-1,3-diene Chemical compound CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE245180C true DE245180C (cg-RX-API-DMAC7.html) |
Family
ID=504157
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT245180D Active DE245180C (cg-RX-API-DMAC7.html) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE245180C (cg-RX-API-DMAC7.html) |
-
0
- DE DENDAT245180D patent/DE245180C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69600746T2 (de) | Herstellung von telechelen Kohlenwasserstoffpolymeren mit Siloxangruppen | |
| DE245180C (cg-RX-API-DMAC7.html) | ||
| DE2042624A1 (de) | Verfahren zur Herstellung von Polymerisationsinitiatoren | |
| DE3240433A1 (de) | Verfahren zur herstellung von homoloymeren und copolymeren von (alpha)-olefinen | |
| DE1542225A1 (de) | Polymerisationsverfahren | |
| DE2254636C3 (de) | Tris-chelate und Verfahren zu ihrer Herstellung | |
| CH622239A5 (cg-RX-API-DMAC7.html) | ||
| DE1921453A1 (de) | Basische Dithienylderivate | |
| DE588708C (de) | Verfahren zur Herstellung halogenierter Butadiene | |
| DE2624204C3 (de) | Methode zur quantitativen Bestimmung von Al-C- und Al-H-Bindungen in Kohlenwasserstoffen | |
| DE1113823B (de) | Verfahren zur Herstellung von trans-1, 4-Polydienen | |
| DE1005952B (de) | Verfahren zur Herstellung von tertiaeren Diaethylenalkoholen | |
| DE2251651A1 (de) | Herstellung von alkinen durch dehydrohalogenierung | |
| DE568759C (de) | Verfahren zur Darstellung von 2-Methyl-5-oxypiperidin | |
| DE865315C (de) | Verfahren zur Herstellung von 3, 5-Dioxyphenylaethanolaminen | |
| DE1000393C2 (de) | Verfahren zur Herstellung von in W-Stellung fluorierten Anisolen | |
| AT240597B (de) | Verfahren zum Polymerisieren von Butadien-1,3 oder seiner durch niedere Alkylgruppen substituierten Derivate | |
| DE1124496B (de) | Verfahren zur Herstellung von tertiaeren Aminen, ihren Saeureadditionssalzen und quaternaeren Ammoniumverbindungen | |
| DE1180944B (de) | Verfahren zur Herstellung von trans-(1, 4)-Polybutadien | |
| DE833806C (de) | Verfahren zur Abtrennung nichtaromatischer Sulfamide aus ihren Herstellungsgemischen | |
| DE1467151A1 (de) | Verfahren zur Herstellung von Natrium- bzw. Kaliumalamat | |
| DE919409C (de) | Verfahren zur Kernchlorierung von 1, 3, 3-Trimethyl-1-phenyl-inden bzw. 1, 3, 3, 6-Tetramethyl-1-(4'-methyl-phenyl)-inden | |
| DE709725C (de) | Verfahren zur Destillation und zum Haltbarmachen von Vinylmethylketon | |
| DE1210191B (de) | Verfahren zur Polymerisation von Butadien-(1, 3) oder dessen niederen Alkylderivatenoder zur Mischpolymerisation von Gemischen dieser Verbindungen | |
| DE639662C (de) | Verfahren zur Reinigung des durch Lichtbogenbehandlung von Kohlenwasserstoffen erhaltenen Rohacetylens |