DE174068C - - Google Patents
Info
- Publication number
- DE174068C DE174068C DE1904174068D DE174068DA DE174068C DE 174068 C DE174068 C DE 174068C DE 1904174068 D DE1904174068 D DE 1904174068D DE 174068D A DE174068D A DE 174068DA DE 174068 C DE174068 C DE 174068C
- Authority
- DE
- Germany
- Prior art keywords
- acetylene
- chloride
- chlorine
- hexachloroethane
- mixture
- 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 - Lifetime
Links
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 16
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 16
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims description 10
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 3
- 150000002506 iron compounds Chemical class 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
- 239000000460 chlorine Substances 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 9
- 238000009835 boiling Methods 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004200 deflagration Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 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
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/02—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT29203D AT29203B (de) | 1904-07-27 | 1905-03-20 | Verfahren zur Darstellung von Tetra- und Hexachloräthan aus Azetylen. |
Publications (1)
Publication Number | Publication Date |
---|---|
DE174068C true DE174068C (enrdf_load_stackoverflow) |
Family
ID=438832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1904174068D Expired - Lifetime DE174068C (enrdf_load_stackoverflow) | 1904-07-27 | 1904-07-27 |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE174068C (enrdf_load_stackoverflow) |
-
1904
- 1904-07-27 DE DE1904174068D patent/DE174068C/de not_active Expired - Lifetime
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE174068C (enrdf_load_stackoverflow) | ||
DE2542496A1 (de) | Verfahren zur herstellung von perfluoralkyljodidtelomeren | |
DE1930594A1 (de) | Verfahren zur Herstellung von 4,4'-Dibromdiphenyl oder -diphenylaether | |
DE1768202A1 (de) | Verfahren zur Herstellung von Arylsulfiden und von neuen Arylsulfidverbindungen | |
DE2756235C2 (de) | Verfahren zur Herstellung von gegebenenfalls substituiertem Benzotrifluorid | |
DE801987C (de) | Verfahren zur Herstellung von Hexachloraethan | |
DE2243811C3 (de) | Verfahren zur Herstellung von Methylformiat | |
DE1034184B (de) | Verfahren zur Herstellung von 1, 3-Propylendiamin | |
DE890339C (de) | Verfahren zur Herstellung von symm. 1, 2, 4, 5-Tetrachlorbenzol aus ª€-Heptachlorcyclohexan | |
AT251557B (de) | Verfahren zur Aufarbeitung von Mischungen aus m- und p-Xylol, die gegebenenfalls o-Xylol und/oder Äthylbenzol enthalten | |
DE234912C (enrdf_load_stackoverflow) | ||
DE1240057B (de) | Verfahren zur Herstellung von 1, 2, 3, 4-Tetra-chlorbutan | |
DE2111723C3 (de) | Verfahren zur Herstellung von Methylvinylketon | |
DE1418334B1 (de) | Verfahren zur Herstellung von 1,2,3,4,7,7-Hexachlorbicyclo[2,2,1]-2,5-heptadien aus Hexachlorcyclopentadien und Acetylen | |
DE973281C (de) | Verfahren zur Chlorwasserstoffabspaltung aus Polychlorcyclohexanen | |
AT212844B (de) | Verfahren zur Herstellung von Azacyclo-2,3-alken-2-chlor-N-carbochlorid durch Reaktion von ω-Lactamen mit Phosgen | |
DE1568007C (de) | Verfahren zur Herstellung von 1,1,2,2 Tetrachlor 1,2 bis (p chlorphenyl) athan | |
DE531579C (de) | Verfahren zur Darstellung von Oxydationsprodukten des Trichloraethylens | |
DE2636381C3 (de) | Verfahren zur Herstellung von Dichlormaleinsäureanhydrid durch Oxidation von Hexachlorbutadien | |
AT233551B (de) | Verfahren zur Herstellung chlorsubstituierter Methylisocyaniddichloride | |
AT225696B (de) | Verfahren zur Herstellung von Bromderivaten aromatischer Kohlenwasserstoffe mit 4 und mehr Bromatomen im Molekül | |
AT160135B (de) | Verfahren zur Herstellung von Tetrachlorkohlenstoff. | |
AT162942B (de) | Verfahren zur Herstellung von Hexachlorcyclohexan | |
DE338281C (de) | Verfahren zur Herstellung von Alkylaethern des Vinylalkohols und seiner Homologen | |
DE568297C (de) | Verfahren zur Herstellung von 1-Phenyl-2, 3-dimethyl-5-pyrazolon |