FR1369785A - Production d'hexafluoroacétone et de pentafluorochloroacétone par conversion catalytique d'une perfluorochloroacétone à plus faible teneur en fluor - Google Patents
Production d'hexafluoroacétone et de pentafluorochloroacétone par conversion catalytique d'une perfluorochloroacétone à plus faible teneur en fluorInfo
- Publication number
- FR1369785A FR1369785A FR948233A FR948233A FR1369785A FR 1369785 A FR1369785 A FR 1369785A FR 948233 A FR948233 A FR 948233A FR 948233 A FR948233 A FR 948233A FR 1369785 A FR1369785 A FR 1369785A
- Authority
- FR
- France
- Prior art keywords
- solution
- perfluorochloroacetone
- pentafluorochloroacetone
- hexafluoroacetone
- fluorine
- 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
- OJUUDWYPNQALHZ-UHFFFAOYSA-N 1-chloro-1,1,3,3,3-pentafluoropropan-2-one Chemical compound FC(F)(F)C(=O)C(F)(F)Cl OJUUDWYPNQALHZ-UHFFFAOYSA-N 0.000 title abstract 4
- VBZWSGALLODQNC-UHFFFAOYSA-N hexafluoroacetone Chemical compound FC(F)(F)C(=O)C(F)(F)F VBZWSGALLODQNC-UHFFFAOYSA-N 0.000 title abstract 3
- 229910052731 fluorine Inorganic materials 0.000 title abstract 2
- 239000011737 fluorine Substances 0.000 title abstract 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title 1
- 230000003197 catalytic effect Effects 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 title 1
- 238000010438 heat treatment Methods 0.000 abstract 5
- 239000003054 catalyst Substances 0.000 abstract 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- 239000000243 solution Substances 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical class CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 abstract 2
- 150000001844 chromium Chemical class 0.000 abstract 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 239000011261 inert gas Substances 0.000 abstract 2
- 230000001376 precipitating effect Effects 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 239000000908 ammonium hydroxide Substances 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 239000011651 chromium Substances 0.000 abstract 1
- 238000004508 fractional distillation Methods 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008188 pellet Substances 0.000 abstract 1
- 239000002244 precipitate Substances 0.000 abstract 1
- 239000011819 refractory material Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/24—Chromium, molybdenum or tungsten
- B01J23/26—Chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22644062A | 1962-09-26 | 1962-09-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
FR1369785A true FR1369785A (fr) | 1964-08-14 |
Family
ID=22848916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR948233A Expired FR1369785A (fr) | 1962-09-26 | 1963-09-20 | Production d'hexafluoroacétone et de pentafluorochloroacétone par conversion catalytique d'une perfluorochloroacétone à plus faible teneur en fluor |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE637698A (de) |
DE (1) | DE1199754B (de) |
ES (1) | ES291865A1 (de) |
FR (1) | FR1369785A (de) |
GB (1) | GB994093A (de) |
NL (1) | NL298216A (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1036870A (en) * | 1964-07-08 | 1966-07-20 | Du Pont | Preparation of fluorinated perhaloaldehydes |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2807646A (en) * | 1955-03-14 | 1957-09-24 | Allied Chem & Dye Corp | Manufacture of chlorofluoroacetones |
DE1057087B (de) * | 1955-03-14 | 1959-05-14 | Allied Chem | Verfahren zur Herstellung von Perchlorfluoracetonen |
-
0
- NL NL298216D patent/NL298216A/ unknown
- BE BE637698D patent/BE637698A/ unknown
-
1963
- 1963-09-20 FR FR948233A patent/FR1369785A/fr not_active Expired
- 1963-09-20 DE DEA44107A patent/DE1199754B/de active Pending
- 1963-09-20 ES ES0291865A patent/ES291865A1/es not_active Expired
- 1963-09-25 GB GB3777463A patent/GB994093A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
ES291865A1 (es) | 1964-01-01 |
BE637698A (de) | |
NL298216A (de) | |
DE1199754B (de) | 1965-09-02 |
GB994093A (en) | 1965-06-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2032098C3 (de) | Verfahren zur Herstellung eines Chromoxidkatalysators zur Fluorierung von Kohlenwasserstoffen | |
JPS63295521A (ja) | 触媒の存在下でのフッ化水素化による1,1,1−トリフルオロ−2,2−ジクロロエタンの製法 | |
JPS61115049A (ja) | 乳酸および乳酸アンモニウムのアクリル酸への接触転化 | |
GB901297A (en) | Process for the production of pentafluoroethane | |
US3595911A (en) | Production of unsaturated carboxylic acids | |
FR1369785A (fr) | Production d'hexafluoroacétone et de pentafluorochloroacétone par conversion catalytique d'une perfluorochloroacétone à plus faible teneur en fluor | |
US3235612A (en) | Manufacture of fluorocarbons | |
JPH03109336A (ja) | 1,1,1,2‐テトラフルオロエタンの製造方法 | |
US3257457A (en) | Production offluoro compounds | |
GB976883A (en) | Improvements in or relating to the manufacture of organic flourine compounds | |
JPS5834457B2 (ja) | フホウワアルデヒドオサンニヘンカンヨウカイリヨウシヨクバイ | |
US3267161A (en) | Chlorination process | |
US2197956A (en) | Vapor phase dehydration of acetylenic alcohols | |
US2601538A (en) | Catalytic isomerization of propylene oxide to propionaldehyde, catalyst therefor, and synthesis of catalyst | |
GB976316A (en) | Process for preparing fluorinated perhalo compounds | |
US2862036A (en) | Preparation of 2,2,3-trichloroheptafluorobutane | |
US2225635A (en) | Preparation of vinyl halides | |
US3333011A (en) | Production of chlorotrifluoroethylene | |
US2653964A (en) | Preparation of nitriles and catalysts therefor | |
US2871274A (en) | Oxybromination of chlorodifluoromethane | |
US3251886A (en) | Production of 4-methylmercaptophenols and 3-isopropyl derivative | |
JPS6244973B2 (de) | ||
GB896068A (en) | Process for the production of chloropentafluoroethane | |
US2451712A (en) | Acrolein and ethylene by pyrolysis of dihydropyran | |
US2042303A (en) | Production of aldehydes |