GB1363521A - Method of producing fluoro-substituted alkyliodide telomers and catalyst therefor - Google Patents
Method of producing fluoro-substituted alkyliodide telomers and catalyst thereforInfo
- Publication number
- GB1363521A GB1363521A GB3198171A GB3198171A GB1363521A GB 1363521 A GB1363521 A GB 1363521A GB 3198171 A GB3198171 A GB 3198171A GB 3198171 A GB3198171 A GB 3198171A GB 1363521 A GB1363521 A GB 1363521A
- Authority
- GB
- United Kingdom
- Prior art keywords
- metal salt
- catalyst
- period
- complex
- ethanolamine
- 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
- 239000003054 catalyst Substances 0.000 title abstract 7
- 150000001351 alkyl iodides Chemical class 0.000 title 1
- 239000002184 metal Substances 0.000 abstract 7
- 229910052751 metal Inorganic materials 0.000 abstract 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- 150000001412 amines Chemical class 0.000 abstract 3
- 229910052718 tin Inorganic materials 0.000 abstract 3
- 229910052719 titanium Inorganic materials 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 239000003463 adsorbent Substances 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003973 alkyl amines Chemical group 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000003841 chloride salts Chemical class 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 150000002823 nitrates Chemical class 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 235000011837 pasties Nutrition 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000741 silica gel Substances 0.000 abstract 1
- 229910002027 silica gel Inorganic materials 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- 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
- C07C17/278—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/10—Complexes comprising metals of Group I (IA or IB) as the central metal
- B01J2531/17—Silver
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/20—Complexes comprising metals of Group II (IIA or IIB) as the central metal
- B01J2531/27—Cadmium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/20—Complexes comprising metals of Group II (IIA or IIB) as the central metal
- B01J2531/28—Mercury
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/30—Complexes comprising metals of Group III (IIIA or IIIB) as the central metal
- B01J2531/31—Aluminium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/40—Complexes comprising metals of Group IV (IVA or IVB) as the central metal
- B01J2531/42—Tin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/40—Complexes comprising metals of Group IV (IVA or IVB) as the central metal
- B01J2531/44—Lead
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/40—Complexes comprising metals of Group IV (IVA or IVB) as the central metal
- B01J2531/46—Titanium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/50—Complexes comprising metals of Group V (VA or VB) as the central metal
- B01J2531/56—Vanadium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/70—Complexes comprising metals of Group VII (VIIB) as the central metal
- B01J2531/72—Manganese
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/845—Cobalt
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/847—Nickel
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2034472A DE2034472C3 (de) | 1970-07-11 | 1970-07-11 | Verfahren zur Herstellung von Perfluor alkyljodidtelomeren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1363521A true GB1363521A (en) | 1974-08-14 |
Family
ID=5776475
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3198171A Expired GB1363521A (en) | 1970-07-11 | 1971-07-07 | Method of producing fluoro-substituted alkyliodide telomers and catalyst therefor |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3883604A (enExample) |
| BE (1) | BE769826A (enExample) |
| DE (1) | DE2034472C3 (enExample) |
| FR (1) | FR2098335B3 (enExample) |
| GB (1) | GB1363521A (enExample) |
| NL (1) | NL7107330A (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1186704B (it) * | 1985-04-04 | 1987-12-16 | Motefluos Spa | Perfluorcalcani e aloperfluoroalcani,loro precursori e loro processo di sintesi |
| US4766103A (en) * | 1986-07-07 | 1988-08-23 | Phillips Petroleum Company | Preparation of 1,4-dichlorobenzene |
| FR2686083B1 (fr) * | 1992-01-13 | 1994-03-25 | Elf Atochem Sa | Synthese d'iodures de perfluoroalkyle. |
| DE4446758A1 (de) * | 1994-12-24 | 1996-06-27 | Hoechst Ag | Metallkatalysierte Herstellung von Perfluoralkyliodid-Telomeren |
| US20040249225A1 (en) * | 2001-10-24 | 2004-12-09 | Tatsuya Hirata | Method an system for recovery of catalysts and process and unit for production of perfluoroalkyl iodide telomers |
| US8212064B2 (en) * | 2008-05-14 | 2012-07-03 | E.I. Du Pont De Nemours And Company | Ethylene tetrafluoroethylene intermediates |
| US8318877B2 (en) * | 2008-05-20 | 2012-11-27 | E.I. Du Pont De Nemours And Company | Ethylene tetrafluoroethylene (meth)acrylate copolymers |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2770659A (en) * | 1952-06-19 | 1956-11-13 | Kellogg M W Co | Telomerization with sulfuryl halide and product thereof |
| US3006973A (en) * | 1959-05-01 | 1961-10-31 | Pennsalt Chemicals Corp | Halogenated organic compounds |
| US3454657A (en) * | 1967-08-24 | 1969-07-08 | Dow Chemical Co | Catalytic synthesis of organic halogen compounds |
| SE353896B (enExample) * | 1967-10-04 | 1973-02-19 | Ciba Geigy Ag |
-
1970
- 1970-07-11 DE DE2034472A patent/DE2034472C3/de not_active Expired
-
1971
- 1971-05-27 NL NL7107330A patent/NL7107330A/xx unknown
- 1971-06-29 FR FR7123766A patent/FR2098335B3/fr not_active Expired
- 1971-07-07 GB GB3198171A patent/GB1363521A/en not_active Expired
- 1971-07-08 US US165849A patent/US3883604A/en not_active Expired - Lifetime
- 1971-07-09 BE BE769826A patent/BE769826A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2098335A3 (enExample) | 1972-03-10 |
| DE2034472B2 (de) | 1973-03-15 |
| DE2034472A1 (de) | 1972-02-10 |
| FR2098335B3 (enExample) | 1973-10-19 |
| DE2034472C3 (de) | 1973-10-25 |
| NL7107330A (enExample) | 1972-01-13 |
| US3883604A (en) | 1975-05-13 |
| BE769826A (fr) | 1972-01-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS5855131B2 (ja) | 線状ポリアルキレンポリアミンの製法 | |
| GB1521101A (en) | Zeolite and method of preparing it | |
| GB1363521A (en) | Method of producing fluoro-substituted alkyliodide telomers and catalyst therefor | |
| KR850004576A (ko) | 니트로 디 아릴아민의 제조방법 | |
| GB1429651A (en) | Manufacture of organic nitriles | |
| ES313102A1 (es) | Un metodo de preparar compuestos de organoestaño. | |
| GB1365782A (en) | Prilled ammonium nitrate composition | |
| GB1203737A (en) | Novel catalysts and their use in cationic polymerisations | |
| ES436502A1 (es) | Procedimiento para la obtencion de anilidas de acido o-ami- nosulfonil-glicolico. | |
| ATE535T1 (de) | Verfahren zum bereiten eines granulierten npk-duengemittels und ein durch dieses verfahren erhaltenes granuliertes npk-duengemittel. | |
| GB1427601A (en) | Quaternary ammonium salts process for the production thereof and their use | |
| US2413623A (en) | Production of vinyl cyanide | |
| GB1351523A (en) | Catalyst and process for producing aromatic nitriles | |
| GB1459685A (en) | Conversion of nitriles to amides | |
| IE35753L (en) | Bis-pyridyl amines | |
| KR900004399A (ko) | 파라핀의 암모산화 및 그 촉매 | |
| US2299222A (en) | Process for the catalytic production of olefin-sulphur dioxide compounds of high molecular weight | |
| GB1523747A (en) | Process for producing methacrolein | |
| GB875984A (en) | A process for the production of n-substituted n-aryl ureas | |
| GB1232831A (enExample) | ||
| GB1219698A (en) | Substituted carbanilides and their use | |
| SU611898A1 (ru) | Способ получени медленнодействующих сложных удобрений | |
| Baldwin et al. | The unsymmetrical coupling of geraniol | |
| GB1486081A (en) | Catalytic process for preparing unsaturated nitriles from olefins ammonia and oxygen and a catalyst therefore | |
| GB1330353A (en) | Anti-microbially active surface-active compositions |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 416 | Proceeding under section 16 patents act 1949 | ||
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |