DE200915C - - Google Patents
Info
- Publication number
- DE200915C DE200915C DENDAT200915D DE200915DA DE200915C DE 200915 C DE200915 C DE 200915C DE NDAT200915 D DENDAT200915 D DE NDAT200915D DE 200915D A DE200915D A DE 200915DA DE 200915 C DE200915 C DE 200915C
- Authority
- DE
- Germany
- Prior art keywords
- magnesium
- solution
- chlorohydrate
- pinene
- 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.)
- Active
Links
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 17
- 229910052749 magnesium Inorganic materials 0.000 claims description 17
- 239000011777 magnesium Substances 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 5
- 150000004792 aryl magnesium halides Chemical class 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 239000011630 iodine Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000003747 Grignard reaction Methods 0.000 description 3
- -1 bornyl iodide magnesium Chemical compound 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 3
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 2
- 150000001350 alkyl halides Chemical class 0.000 description 2
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 2
- 125000005998 bromoethyl group Chemical group 0.000 description 2
- 229930006739 camphene Natural products 0.000 description 2
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002681 magnesium compounds Chemical class 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- SRXLZGNFCCYTNZ-UHFFFAOYSA-N [Mg]CCI Chemical compound [Mg]CCI SRXLZGNFCCYTNZ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001351 alkyl iodides Chemical class 0.000 description 1
- 150000001500 aryl chlorides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001502 aryl halides Chemical class 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- DCUKIPCLKPKATJ-UHFFFAOYSA-N chloromethylbenzene;magnesium Chemical compound [Mg].ClCC1=CC=CC=C1 DCUKIPCLKPKATJ-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- VXWPONVCMVLXBW-UHFFFAOYSA-M magnesium;carbanide;iodide Chemical compound [CH3-].[Mg+2].[I-] VXWPONVCMVLXBW-UHFFFAOYSA-M 0.000 description 1
- FRIJBUGBVQZNTB-UHFFFAOYSA-M magnesium;ethane;bromide Chemical compound [Mg+2].[Br-].[CH2-]C FRIJBUGBVQZNTB-UHFFFAOYSA-M 0.000 description 1
- 239000008096 xylene 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
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/02—Magnesium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE200915C true DE200915C (cs) |
Family
ID=463510
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT200915D Active DE200915C (cs) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE200915C (cs) |
-
0
- DE DENDAT200915D patent/DE200915C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1085508B (de) | Verfahren zur Herstellung von Polyphosphornitrilchloriden | |
| DE200915C (cs) | ||
| EP0253214A1 (de) | Verfahren zur Herstellung von Chlorcarbonsäurechloriden | |
| DE2324390C2 (de) | Verfahren zur Herstellung von Derivaten des 2,2-Dichlor- bzw. 2,2-Dibromcyclopropans | |
| DE1287062B (de) | Verfahren zur Gewinnung von hoehermolekularen ª‡-Olefinen | |
| DE4301554C1 (de) | Verfahren zur Herstellung von Diethoxymethan | |
| DE189476C (cs) | ||
| DE118537C (cs) | ||
| DE193177C (cs) | ||
| DE2233489C3 (de) | Verfahren zur Herstellung von Octachlordipropyläther | |
| DE1210788B (de) | Verfahren zur Herstellung von gesaettigten Fettsaeuren oder ihren Magnesiumsalzen | |
| DE230172C (cs) | ||
| DE1197075B (de) | Verfahren zur Herstellung von Cyanformamid | |
| DE977532C (de) | Verfahren zur Herstellung von Alkylzinnverbindungen neben Alkylzinnhalogenverbindungen | |
| DE214044C (cs) | ||
| DE2137546C3 (de) | Verfahren zur Herstellung von 17alpha Athjnyl, Methyl und Vinyl 17beta Acetyloxysteroiden der Androstan bzw Ostranreihe | |
| DE2648965C2 (de) | Verfahren zur Herstellung von Chlormethylthiocyanat | |
| CH624668A5 (cs) | ||
| DE108223C (cs) | ||
| DE910410C (de) | Verfahren zur Herstellung von Vinylchlorid | |
| DE120865C (cs) | ||
| DE84336C (cs) | ||
| DE1568325A1 (de) | Stabilisierung von Aluminiumalkoxyden | |
| DE898897C (de) | Verfahren zur Herstellung von primaeren und sekundaeren ?-Alkenylmalonsaeureestern oder -cyanessigsaeureestern | |
| DE2556206C3 (de) | Verfahren zur Herstellung von Terephthalaldehyd |