GB907148A - Improved process for carrying out telomerizing reactions - Google Patents
Improved process for carrying out telomerizing reactionsInfo
- Publication number
- GB907148A GB907148A GB2521759A GB2521759A GB907148A GB 907148 A GB907148 A GB 907148A GB 2521759 A GB2521759 A GB 2521759A GB 2521759 A GB2521759 A GB 2521759A GB 907148 A GB907148 A GB 907148A
- Authority
- GB
- United Kingdom
- Prior art keywords
- liquid
- telogen
- olefine
- walls
- gaseous
- 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
Links
- 238000006243 chemical reaction Methods 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 2
- 239000007788 liquid Substances 0.000 abstract 5
- 230000003797 telogen phase Effects 0.000 abstract 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 abstract 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- POJPQMDDRCILHJ-UHFFFAOYSA-N 1,1,1,2,2,2-hexabromoethane Chemical compound BrC(Br)(Br)C(Br)(Br)Br POJPQMDDRCILHJ-UHFFFAOYSA-N 0.000 abstract 1
- APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 abstract 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- ZHAORBUAOPBIBP-UHFFFAOYSA-N 2,2-dibromo-1-phenylethanone Chemical compound BrC(Br)C(=O)C1=CC=CC=C1 ZHAORBUAOPBIBP-UHFFFAOYSA-N 0.000 abstract 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 abstract 1
- HLHNOIAOWQFNGW-UHFFFAOYSA-N 3-bromo-4-hydroxybenzonitrile Chemical compound OC1=CC=C(C#N)C=C1Br HLHNOIAOWQFNGW-UHFFFAOYSA-N 0.000 abstract 1
- HGINADPHJQTSKN-UHFFFAOYSA-M 3-ethoxy-3-oxopropanoate Chemical compound CCOC(=O)CC([O-])=O HGINADPHJQTSKN-UHFFFAOYSA-M 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000110 cooling liquid Substances 0.000 abstract 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 abstract 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 abstract 1
- 239000012263 liquid product Substances 0.000 abstract 1
- 229910001507 metal halide Inorganic materials 0.000 abstract 1
- 150000005309 metal halides Chemical class 0.000 abstract 1
- VHFUHRXYRYWELT-UHFFFAOYSA-N methyl 2,2,2-trichloroacetate Chemical compound COC(=O)C(Cl)(Cl)Cl VHFUHRXYRYWELT-UHFFFAOYSA-N 0.000 abstract 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/275—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of hydrocarbons and halogenated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
<PICT:0907148/III/1> Apparatus suitable for telomerization reactions (see Group IV(b)) comprises a vessel 4 (preferably tubular and vertical) with a means for controlling the temperature of the reactants by heat exchange through the walls thereof, e.g. the jacket 8 for a cooling liquid and a device for causing a telogen in liquid form (see Group IV(b)) to form a liquid film over the inside walls of the vessel, e.g. the rotary basket 11 on shaft 20, the liquid being preheated in heater 3. Gaseous olefine is fed under pressure through piping 7. Liquid products are discharged through 13, cooled in 14, and passed to separator 15 for recycle of gaseous olefine via 16 and to distiller 17 for recycle of telogen via 19. Reaction product is taken off at 18.ALSO:Telomers are prepared from gaseous olefines by a process in which the telogen, together with a polymerisation catalyst, is fed to the reaction chamber wherein the telomerisation is to take place under superatmospheric pressure, in the form of a liquid film running at the periphery of said chamber, in immediate contact with the walls, through which heat exchange takes place. Ethylene and propylene are specified as the olefine. The telogen may itself be liquid at room temperature to reaction temperature (such as carbon tetrachloride, chloroform, monochloroacetic acid, trichloroacetic acid, ethyl bromoacetate, mono- and diethyl malonate, methyl formate and methyl trichloroacetate), or may be dissolved in a suitable solvent (such as tribromoacetic acid and hexachloroethane in pentane, octane or hexadecane; and hexabromoethane, dibromoethane and dibromoacetophenone in dioxane). Suitable catalysts are acyl oxides such as benzoyl peroxide; azoisobutyronitrile; and metal halides.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT1211758 | 1958-08-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB907148A true GB907148A (en) | 1962-10-03 |
Family
ID=11139464
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2521759A Expired GB907148A (en) | 1958-08-09 | 1959-07-22 | Improved process for carrying out telomerizing reactions |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE581001A (en) |
DE (1) | DE1154480B (en) |
FR (1) | FR1235723A (en) |
GB (1) | GB907148A (en) |
NL (1) | NL241574A (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1084724B (en) * | 1956-01-13 | 1960-07-07 | Degussa | Continuous process for carrying out telomerizations |
-
0
- BE BE581001D patent/BE581001A/xx unknown
- NL NL241574D patent/NL241574A/xx unknown
-
1959
- 1959-07-22 GB GB2521759A patent/GB907148A/en not_active Expired
- 1959-08-04 FR FR802011A patent/FR1235723A/en not_active Expired
- 1959-08-04 DE DES64288A patent/DE1154480B/en active Pending
Also Published As
Publication number | Publication date |
---|---|
NL241574A (en) | |
DE1154480B (en) | 1963-09-19 |
FR1235723A (en) | 1960-07-08 |
BE581001A (en) |
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