Abstract:
Carbonyl dihalides COFX (where X is F, Cl or Br) are obtained by reaction of a perhalomethane CFXYZ (where Y and Z are Cl or Br) with sulfur trioxide. The reaction may be catalyzed by the presence of sulfuric acid and/or heavy metal salts such as mercury salts.
Abstract:
The invention relates to a process for the preparation of 2-H-heptafluoropropane, wherein hexafluoropropene is reacted with hydrogen fluoride in the presence of a weakly basic ion exchanger whose reactive centers comprise tertiary amino groups.
Abstract:
of the disclosures HOE 89/F 008 A process for the continuous oligomerization of hexafluoropropene oxide A continuous process for the preparation of perfluorinated carbonyl fluorides from hexafluoropropene oxide (HFPO), in which HFPO is continuously oligomerized in a catalyst solution in devices which allow separation of the heavy product phase from the catalyst phase during the reaction, is described. Different oligomer distributions can be achieved by choice of the catalyst and different operating temperatures. The reaction itself takes place always in the substantial absence of the product which is formed, and achieves a considerable saving in time.
Abstract:
1,2,2,2-TETRAFLUORETHYL-FLUOROMETHYL ETHER AND PROCESS FOR PREPARING IT The invention relates to 1,2,2,2-tetrafluorethyl-fluoromethyl ether, to a process for preparing it and to its use as inhalation anesthetic.
Abstract:
Process for the preparation of halogenated aromatic compounds of the formula … … in which Hal denotes fluorine, chlorine or bromine and… Z denotes an aromatic group,… characterised in that a halobenzene of the formula C6H5Hal (II) is reacted under anhydrous conditions with a bis-acid halide of the formula Hal-CO-Z-CO-Hal (III) in a molar ratio of at least 2:1 in the presence of haloalkanesulphonic acids of the formula Y(CnX2n)SO3H (IV), where in the formulae II and III Hal and Z have the meaning given previously and Y denotes fluorine or hydrogen, X denotes fluorine and/or chlorine and n denotes an integer from 1 to 10, where at least one X stands for fluorine. … The invention further relates to the use of compounds of the formula I, preferably of 1,4-bis(4-fluorobenzoyl)benzene and of 1,4-bis(4-chlorobenzoyl)benzene, in the form of a clear solution in diphenyl sulphone, which has been obtained by treatment with a solid base, preferably Na2CO3, K2CO3 or MgO, for the preparation of polycondensates.
Abstract:
HOE 89/F 101 of the disclosure Hexafluoroisopropyl-containing monomers, processes for their preparation, and their use Compounds of the formula I (I) can be prepared by various procesæ steps from 2-(4-methylphenyl)-2-hexafluoroisopropanol. Hexafluoroisopropyl-containing monomers are important starting compounds in the preparation of linear polycarboxamides and polycarboximides.
Abstract:
This invention is directed to .omega.-fluorosulfato-perfluoro-(2-methyl-alkan-3-one) of the formula V FS020-(CF2)m-?-CF(CF3)2 wherin m = a number from 1 to 10. The compounds of the invention are intermediates for the preparation of perfluoroisopropylketoearboxylie acid flourides. These eompounds are used for the preparation of perfluorinated ketocarboxylic acid esters which have an isopropyl radical adjacent to the keto group and are in turn, in particular, valuable heat transfer fluids and surface-active agents with a high stability to chemicals and heat.
Abstract:
Process for the addition of HF to halogenated alkenes The invention relates to a process for the addition of HF to halogenated alkenes by reacting these with at least one hydrofluoride of the formula [B.cndot.n HF], in which B is an organic nitrogen base and n is as integer or fraction .ltoreq. 4, it being intended that the reaction of perfluoroiso- butene CF2=C(CF3)2 is excluded.
Abstract:
of the disclosure: Substituted phenyl .alpha.-fluoroacrylates Certain esters of .alpha.-fluoroacrylic acid are accessible by hydrolyzing .alpha.-hydroxymethyl .alpha.-fluoromalonic acid esters and subsequently decarboxylating the hydrolysis product The phenyl .alpha.-fluoroacrylates which are substituted on the phenyl radical can be prepared by hydroxymethylating dimethyl .alpha.-fluoromalonate, decarboxylating and dehydrating the resulting dimethyl .alpha.-hydroxymethyl-.alpha.-fluoro-malonate and esterifying the resulting .alpha.-fluoroacrylic acid with substituted phenols. The substituted phenyl .alpha.-fluoroacrylates are colorless liquids or colorless solids which can be polymerized. They are suitable for use as a starting material for the preparation of fluorine polymers.