# US 5,710,342 A · Process for preparing carbonyl compounds by catalysed oxidation of olefins and catalysts present microemulsions > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 5,710,342 A - Document ID: US5710342A - Status: Granted - Kind: A - Application number: 08/568,054 - Filed: 1995-12-06 - Granted: 1998-01-20 - Earliest claimed: 1994-12-15 - Assignees: Bayer Aktiengesellschaft - Inventors: Laszlo Imre; Reinhard Schomacker; Judit Daun - Web page: https://patentgrep.com/patent/US5710342A ## CPC - C07C 45/34: in unsaturated compounds - C07C 45/35: in propene or isobutene - C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS ## Abstract Carbonyl compounds can be prepared by catalytic oxidation of olefins with oxygen or oxygen-containing gases in a microemulsion (ME) as reaction medium and catalyst support. The catalysts present in ME and used for this purpose are characterized by a content of 0.0001-10% by weight of a Pd compound and by a content of 0.0005-20% by weight of a subgroup metal compound or a quinone, based on the total weight of the catalysts present in the ME. ## Claims ### Claim 1 A process for preparing a carbonyl compound of the formula ##STR4## by catalytic oxidation of an olefin of the formula ##STR5## where, in the formulae R.sup.1, R.sup.2 and R.sup.3 are, independently of one another, hydrogen; straight-chain or branched C.sub.1 -C.sub.8 -alkyl which is unsubstituted or monosubstituted or disubstituted by halogen, hydroxy, cyano, COO--C.sub.1 -C.sub.4 -alkyl, CO--C.sub.1 -C.sub.4 -alkyl, SO.sub.2 --O--C.sub.1 -C.sub.2 -alkyl or phenyl; or phenyl or naphthyl which are unsubstituted or monosubstituted or disubstituted by halogen, hydroxy, nitro, cyano, C.sub.1 -C.sub.4 -alkyl, COO--C.sub.1 -C.sub.4 -alkyl, CO--C.sub.1 -C.sub.4 -alkyl or SO.sub.2 --O--C.sub.1 -C.sub.4 -alkyl, and R.sup.1 and R.sup.3 or R.sup.2 and R.sup.3 can further more together form an alkylene chain .paren open-st.CH.sub.2 .paren close-st..sub.m where m=3-10 and 1-2 of the alkylene chain carbon atoms can be substituted by halogen, hydroxy, C.sub.1 -C.sub.4 -alkyl, COO--C.sub.1 -C.sub.4 -alkyl, CO--C.sub.1 -C.sub.4 -alkyl, SO.sub.2 --O--C.sub.1 -C.sub.4 -alkyl or phenyl, by an oxygen or oxygen-containing gas, wherein the oxidation is carried out at 0.degree.-200.degree. C. and 0.2-200 bar in the presence of a catalyst system comprising a palladium compound and one or more reoxidizing agents from the group of compounds of further subgroup metals and quinones, in a microemulsion as reaction medium and catalyst support, wherein the size of the droplets of said microemulsion range from 5 to 100 nm. ### Claim 2 (depends on 1) The process of claim 1, wherein the oxidation is carried out at 0.degree. to 120.degree. C. ### Claim 3 (depends on 2) The process of claim 2, wherein the oxidation is carried out at 10.degree. to 80.degree. C. ### Claim 4 (depends on 3) The process of claim 3, wherein the oxidation is carried out at 15.degree. to 40.degree. C. ### Claim 5 (depends on 1) The process of claim 1, wherein the oxidation is carried out at 0.5 to 100 bar. ### Claim 6 (depends on 5) The process of claim 5, wherein the oxidation is carried out at 1 to 10 bar. ### Claim 7 (depends on 1) The process of claim 1, wherein the microemulsion used is a single-phase system comprising (i) 1-20% by weight of water, (ii) 60-97% by weight of one or more organic components from the group of olefins to be reacted and organic solvents and (iii) 2-20% by weight of one or more surfactants from the group of ionic and nonionic surfactants, where all figures are based on the total weight of the microemulsion. ### Claim 8 (depends on 7) The process of claim 7, wherein the number of surfactants (iii) is 1-3. ### Claim 9 (depends on 7) The process of claim 7, wherein surfactants used are those from the group of n-(C.sub.8 -C.sub.18)-alkyl-sulphonates, n-(C.sub.8 -C.sub.18)-alkyl-benzenesulphonates, n-(C.sub.8 -C.sub.18)-alkyl-trimethyl ammonium salts, di-(n-(C.sub.8 -C.sub.18)-alkyl-dimethyl-ammonium salts, n-(C.sub.8 -C.sub.18)-alkyl-carboxylates, oligoethylene oxide (EO.sub.2-30)-mono-n-(C.sub.6 -C.sub.18)-alkyl ethers, n-(C.sub.8 -C.sub.18)-alkyl-dimethylamine oxides, n-(C.sub.8 -C.sub.18)-alkyl-dimethyl-phosphine oxides or oligoethylene oxide(EO.sub.2-30)-mono-aryl ethers. ### Claim 10 (depends on 1) The process of claim 1, wherein reoxidizing agents used are one or more subgroup metals from the group of iron, cobalt, nickel, copper, chromium, tin, antimony, cerium, rhodium, platinum, gold, preferably iron or copper. ### Claim 11 (depends on 10) The process of claim 10, wherein the catalyst contains PdCl.sub.2 or Pd(NO.sub.3).sub.2 and Fe(NO.sub.3).sub.3 or CuCl.sub.2. ### Claim 12 (depends on 1) The process of claim 1, wherein the Pd compound of the catalyst makes up 0.0005-10% by weight of the microemulsion and the subgroup metal compounds make up 0.0001-20% by weight of the microemulsion. ### Claim 13 (depends on 12) The process of claim 12, wherein the Pd compound makes up 0.05-1% by weight of the microemulsion and the subgroup metal compound is present in a proportion 2-100 times that of the Pd compound. ### Claim 14 (depends on 1) The process of claim 1, wherein the olefin used has the formula ##STR6## where R.sup.11 and R.sup.12 are, independently of one another, hydrogen; straight-chain or branched C.sub.1 -C.sub.4 -alkyl which is unsubstituted or substituted by halogen, hydroxy, COO--CH.sub.3, CO--CH.sub.3 or phenyl; or phenyl which is unsubstituted or substituted by halogen, hydroxy, nitro, CH.sub.3, C.sub.2 H.sub.5, COO--CH.sub.3 or CO--CH.sub.3, and R.sup.13 is hydrogen or methyl, and R.sup.11 and R.sup.13 or R.sup.12 and R.sup.13 can together represent trimethylene, tetramethylene or pentamethylene.