GB887691A - Aromatic fluorine compounds employed in the production of polymeric gums - Google Patents
Aromatic fluorine compounds employed in the production of polymeric gumsInfo
- Publication number
- GB887691A GB887691A GB462860A GB462860A GB887691A GB 887691 A GB887691 A GB 887691A GB 462860 A GB462860 A GB 462860A GB 462860 A GB462860 A GB 462860A GB 887691 A GB887691 A GB 887691A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pentafluorophenol
- pyridine
- production
- fluorine compounds
- compounds employed
- 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
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
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
-
- 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
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/2632—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions involving an organo-magnesium compound, e.g. Grignard synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/02—Monocyclic aromatic halogenated hydrocarbons
- C07C25/13—Monocyclic aromatic halogenated hydrocarbons containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
- C07C37/02—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis by substitution of halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/64—Preparation of O-metal compounds with O-metal group bound to a carbon atom belonging to a six-membered aromatic ring
- C07C37/66—Preparation of O-metal compounds with O-metal group bound to a carbon atom belonging to a six-membered aromatic ring by conversion of hydroxy groups to O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/24—Halogenated derivatives
- C07C39/26—Halogenated derivatives monocyclic monohydroxylic containing halogen bound to ring carbon atoms
- C07C39/27—Halogenated derivatives monocyclic monohydroxylic containing halogen bound to ring carbon atoms all halogen atoms being bound to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/24—Halogenated derivatives
- C07C39/44—Metal derivatives of an hydroxy group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Pentafluorophenol is produced by heating hexafluorobenzene with solid or alcoholic potassium hydroxide in the presence of pyridine, or a mixture of pyridine and dioxane, and then acidifying the cooled reaction-mixture to liberate pentafluorophenol from its potassium salt. When alcoholic potassium hydroxide is used in the reaction, a large yield of tetrafluorodihydroxybenzene and small amounts of pentafluorophenetole and tetrafluorodiethoxybenzene are produced, in addition to pentafluorophenol. Examples 7 and 8 relate to the preparation of the sodium, ammonium and silver salts of pentafluorophenol. When heated at 200 DEG C.-350 DEG C., these salts give gums of the formula C6F5-(O-C6H4)y-OX where X=Na, Ag &c. and y is 10 to 15. Pentafluorophenylbenzoate is formed when pentafluorophenol is reacted with benzoyl chloride in pyridine. Example 6 describes the preparation of pentachlorotoluene by reacting hexafluorobenzene with methyllithium in ethereal solution.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79292459A | 1959-02-12 | 1959-02-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB887691A true GB887691A (en) | 1962-01-24 |
Family
ID=25158497
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB462860A Expired GB887691A (en) | 1959-02-12 | 1960-02-10 | Aromatic fluorine compounds employed in the production of polymeric gums |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1249579A (en) |
GB (1) | GB887691A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0221635A1 (en) * | 1985-09-13 | 1987-05-13 | Imperial Chemical Industries Plc | Fluoro alcohols and insecticidal esters thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1907879C3 (en) * | 1969-02-17 | 1978-11-02 | Union Rheinische Braunkohlen Kraftstoff Ag, 5047 Wesseling | Process for the preparation of alkyldihydroxybenzenes |
-
1960
- 1960-02-10 GB GB462860A patent/GB887691A/en not_active Expired
- 1960-02-12 FR FR818376A patent/FR1249579A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0221635A1 (en) * | 1985-09-13 | 1987-05-13 | Imperial Chemical Industries Plc | Fluoro alcohols and insecticidal esters thereof |
Also Published As
Publication number | Publication date |
---|---|
FR1249579A (en) | 1960-12-30 |
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