Abstract:
NOVEL FLUOROPERHALODIAZOLEFINE ARE PREPARED BY REACTING A FLUOROPERHALOALKYLIDENE IMINE WITH A FLUOROPERHALOAZAOLEFIN IN AN APROTIC, POLAR LIQUID REACTION MEDIUM IN THE PRESENCE OF AN IONIZABLE FLUORIDE SALT. FOR EXAMPLE, PERFLUORO-2,4,4,6-TETRAMETHYL-3,5-DIAZA -25-HEPTADIENE IS PREPARED BY REACTING HEXAFLUOROISOPROYLIDENE IMINE WITH PERFLUORO-2,4-DIMETHYL-3-AZA-2-PENTENE IN ACETONITRILE IN THE PRESENCE OF POTASSIUM FLUORIDE. THE FLUOROPERHALODIAZAOLEFINS ARE USEFUL AS LIQUID DIELECTRICS AND AS INTERMEDIATES IN THE PREPARATION OF P OTHER FLUORINATED ORGANIC COMPOUNDS.
WHEREIN R IS AN ALKYLENE GROUP OF 1 TO 12 CARBON ATOMS, AN ALKYLENE GROUP OF 2 TO 12 CARBON ATOMS, OR A PHENYLENE GROUP, Q IS AN INTEGER FROM 1 TO 6, AND RF IS A RADICAL HAVING THE FORMULA
Y(CF2)5(CH2)T-
WHEREIN S IS AN INTEGER FROM 1 TO 16, T IS AN INTEGER NOT GREATER THAN S FROM 0 TO 8, WITH THE SUM OF S PLUS T BEING FROM 1 TO 20, AND Y IS SELECTED FROM THE GROUP CONSISTING OF F3C- AND RADICALS HAVING THE FORMULA
R1-CF(-R2)-CF(-O(-))-CF(-R1)-R2 NOVEL FLUOROCARBON AMIDES USEFUL AS OIL- AND WATERREPELLENT AGENTS HAVE THE FORMULA
WHEREIN R1 AND R2 ARE FLUORINE OR PERFLUOROALKYL GROUPS HAVING FROM 1 TO 9 CARBON ATOMS, WITH NOT MORE THAN THREE OF THE R1 AND R2 GROUPS BEING PERFLUOROALKYL GROUPS.
Abstract:
FLUOROPERHALOAZAOLEFINS ARE PREPARED BY REACTING A FLUOROPERHALOALKYL ISOCYANATE WITH A FLUOROPERHALOALKOXIIDE. FOR EXAMPLE, PERFLUORO-2,4-DIMETHYL-3-AZA-2-PENTENE IS PREPARED BY REACTING HEXAFLUOROISOPROPYL ISOCYANATE WITH POTASSIUM HEPTAFLUOROISOPROPOXIDE. THE FLUOROPERHALOAZAOLEFINS ARE USEFUL AS LIQUID DIELECTRICS AND AS INTERMEDIATES IN THE PREPARATION OF OTHER FLUORINATED ORGANIC COMPOUNDS.
Abstract:
Novel fluorocarbon amides useful as oil- and water-repellant agents have the formula
WHEREIN R is an alkyl diradical of one to 12 carbon atoms, an alkylene diradical of two to 12 carbon atoms, or a phenyl diradical; q is an integer from 1 to 6; and Rf is a radical having the formula
Abstract:
WHEREIN Z1 IS Y1 AS DEFINED ABOVE OR CHLORINE, BROMINE OR IODINE, WITH AN IONIZABLE FLUORIDE SALT CAPABLE OF FORMING AN ALCOHOLATE SALT WITH THE CARBONYL COMPOUND AND BEING SELECTED FROM THE GROUP CONSISTING OF POTASSIUM FLUORIDE, RUBIDIUM FLUORIDE, CESIUM FLUORIDE, SILVER FLUORIDE, AND TETRA (LOWER ALKYL) AMMONIUM FLUORIDES IN THE PRESENCE OF AN APROTIC, POLAR, LIQUID REACTION MEDIUM, THEREAFTER REACTING SAID ALCOHOLATE SALT WITH A CYANOGEN HALIDE, AND WHEREIN LESS THAN 1 MOLE OF CYANOGEN HALIDE IS ADDED TO THE REACTION MIXTURE FOR EACH MOLE OF CARBONYL COMPOUND AND FLUORIDE SALT EMPOLYED AND SEPARATING THE RESULTING FLUOROPERHALOAZAOLEFIN FROM THE REACTION MIXTURE.
Z1-CO-Z2
WHEREIN X IS FLUORINE, CHLORINE OR BROMINE AND M IS 0 TO 6, OR THE FORMULA -CF(CFX)N WHEREIN X IS FLUORINE, CHLORINE OR BROMINE AND N IS 3 TO 5, WHICH PROCESS COMPRISES REACTING, UNDER SUBSTANTIALLY ANHYDROUS CONDITIONS AT A TEMPERATURE BELOW 200*C, A CARBONYL COMPOUND HAVING THE FORMULA
CF2X(CFX)M-
WHEREIN Y1 AND Y2 ARE INDEPENDENTLY FLUORINE OR FLUORO: PERHALOALKYL RADICALS HAVING EITHER THE FORMULA
F-C(-Y1)(-Y2)-N=C(-Y1)-Y2
1. A PROCESS FOR PREPARING FLUOROPERHALOAZAOLEFINS HAVING THE FORMULA
Abstract:
FLUOROPERHALOALKYL ISOCYANATES ARE PREPARED BY REACTING THE CORRESPONDING FLUOROPEHALKOALKYLIDENE IMINE WITH CARBONYL FLUORIDE IN THE PRESENCE OF AN IONIZABLE FLUORIDE SALT.
Abstract:
FLUOROPERHALOALKYLIDENE IMINES HAVING THE FORMULA Y1Y2C=NH, WHEREIN Y1 AND Y2 ARE FLUORINE OR FLUOROPERHALOALKYL RADICALS, ARE PREPARED BY HYDROLYZING THE CORRESPONDING FLUOROPERHALOALKYL ISOCYANATE HAVING THE FORMULA Y1Y2FCNCO WITH WATER IN THE FORM OF A HYDRATE SUCH AS HEXAFLUOROACETONE MONOHYDRATE. THE FLUOROPERHALOALKYLIDENE IMINES ARE USEFUL AS INTERMEDIATES IN THE PREPARATION OF OTHER FLUORINATED COMPOUNDS.