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| Number | Title | Issue Date |
| 6784327 | Process for the production of fluorinated organic compounds and fluorinating agents A process for the production of a fluorinated organic compound, characterized by fluorinating an organic compound having a hydrogen atoms using IF5; and a novel fluorination process for fluorinating an organic compound having a hydrogen atoms by using a f... | 08/31/2004 |
| 6297205 | Monohydric alcohol-free transparent moisturizing bar soap A monohydric alcohol-free, transparent, moisturizing bar soap having a high humectant solvent content. The formulation includes: (i) from about 38% to about 96% of one or more humectant solvents and (ii) from about 3% to about 20% of insoluble and/or solu... | 10/02/2001 |
| 6008407 | Method of preparing fluoroaromatic compounds The present invention provides a method of preparing ortho-difluorobenzene derivatives, which comprises (a) providing a mixture of cyclohexenes by reacting chlorotrifluoroethylene (CTFE) and 1.3-diene in a flow reactor and distilling the resultant, and (b... | 12/28/1999 |
| 5026929 | Synthesis of highly fluorinated aromatic compounds A process is disclosed for making a highly fluorinated aromatic compound by contacting a perfluorocycloalkane, such as perfluorodecahydronaphthalene, with a complex of a metal from Groups IA and IIA of the Periodic Table and an organic electron acceptor. ... | 06/25/1991 |
| 4968830 | Aromatization process Halogen substituted aromatic compounds of the formula ##STR1## wherein Y is selected from the group CO2 H, COF, COCl, COBr, CF3, CN, NCO, or F, and X and X' are independently hydrogen or a halogen selected from the group F-, Cl-... | 11/06/1990 |
| 4754084 | Preparation of substituted fluorobenzenes Substituted fluorobenzenes are produced by pyrolyzing vinylfluorocyclobutanes at a temperature of 250°-450° C. in the presence of activated carbon or certain metal oxides or mixtures of metal oxides.... | 06/28/1988 |
| 4390740 | Process for preparing fluorobenzene Monofluorobenzene is prepared in a good yield by reacting cyclopentadiene or its dimer of the formula: ##STR1## with fluorohalomethane of the formula: wherein Xs are, same or different, halogen atoms in the presence of a phase transfer catalyst and a... | 06/28/1983 |
