ES267213A1 - Procedimiento para la obtenciën de ciclohexanona a partir de ciclohexanol - Google Patents
Procedimiento para la obtenciën de ciclohexanona a partir de ciclohexanolInfo
- Publication number
- ES267213A1 ES267213A1 ES0267213A ES267213A ES267213A1 ES 267213 A1 ES267213 A1 ES 267213A1 ES 0267213 A ES0267213 A ES 0267213A ES 267213 A ES267213 A ES 267213A ES 267213 A1 ES267213 A1 ES 267213A1
- Authority
- ES
- Spain
- Prior art keywords
- acid
- cyclohexanol
- carbonate
- zinc oxide
- cyclohexanone
- 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
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 title abstract 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 title abstract 4
- 238000004519 manufacturing process Methods 0.000 title 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 2
- 239000012535 impurity Substances 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000011667 zinc carbonate Substances 0.000 abstract 2
- 229910000010 zinc carbonate Inorganic materials 0.000 abstract 2
- 235000004416 zinc carbonate Nutrition 0.000 abstract 2
- 239000011787 zinc oxide Substances 0.000 abstract 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 238000006356 dehydrogenation reaction Methods 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 239000001095 magnesium carbonate Substances 0.000 abstract 1
- 239000000395 magnesium oxide Substances 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 235000019260 propionic acid Nutrition 0.000 abstract 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
- 229940005605 valeric acid Drugs 0.000 abstract 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/002—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by dehydrogenation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH859660A CH392495A (de) | 1960-07-28 | 1960-07-28 | Verfahren zur Herstellung von Cyclohexanon aus Cyclohexanol |
Publications (1)
Publication Number | Publication Date |
---|---|
ES267213A1 true ES267213A1 (es) | 1961-11-01 |
Family
ID=4342414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES0267213A Expired ES267213A1 (es) | 1960-07-28 | 1961-05-06 | Procedimiento para la obtenciën de ciclohexanona a partir de ciclohexanol |
Country Status (8)
Country | Link |
---|---|
US (1) | US3350456A (en, 2012) |
BE (1) | BE605777A (en, 2012) |
CH (1) | CH392495A (en, 2012) |
DE (1) | DE1296625B (en, 2012) |
ES (1) | ES267213A1 (en, 2012) |
GB (1) | GB947112A (en, 2012) |
NL (2) | NL259810A (en, 2012) |
SE (1) | SE303130B (en, 2012) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4670605A (en) * | 1985-05-31 | 1987-06-02 | Industrial Technology Research Institute | Process and catalyst for the conversion of cyclohexanol to cyclohexanone |
DE19609954A1 (de) * | 1996-03-14 | 1997-09-18 | Basf Ag | Verfahren zur Dehydrierung von sekundären cyclischen Alkoholen |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1895528A (en) * | 1926-06-24 | 1933-01-31 | Du Pont | Catalytic dehydration and dehydrogenation process |
US1892011A (en) * | 1929-06-14 | 1932-12-27 | Firm Rheinische Kampfer Fabrik | Process for the production of ketones from secondary alcohols |
US2083877A (en) * | 1935-09-18 | 1937-06-15 | Shell Dev | Dehydrogenation of alcohols |
US2552300A (en) * | 1947-09-20 | 1951-05-08 | Allied Chem & Dye Corp | Catalytic conversion of cyclohexyl formate to cyclohexanone |
US2549844A (en) * | 1948-08-23 | 1951-04-24 | Standard Oil Dev Co | Dehydrogenation catalyst |
DE970684C (de) * | 1951-04-15 | 1958-10-23 | Hoechst Ag | Verfahren zur Herstellung von Cyclohexanon durch katalytische Dehydrierung von Cyclohexanol |
DE1161558B (de) * | 1959-12-14 | 1964-01-23 | Halcon International Inc | Verfahren zur Herstellung von Cyclohexanon |
US3149166A (en) * | 1959-12-28 | 1964-09-15 | Basf Ag | Process for the production of pure cyclohexanone |
-
0
- NL NL122629D patent/NL122629C/xx active
- NL NL259810D patent/NL259810A/xx unknown
-
1960
- 1960-07-28 CH CH859660A patent/CH392495A/de unknown
- 1960-09-26 DE DEJ18764A patent/DE1296625B/de active Pending
-
1961
- 1961-05-06 ES ES0267213A patent/ES267213A1/es not_active Expired
- 1961-05-15 SE SE5086/61A patent/SE303130B/xx unknown
- 1961-06-14 GB GB21517/61A patent/GB947112A/en not_active Expired
- 1961-07-05 BE BE605777A patent/BE605777A/fr unknown
-
1964
- 1964-02-11 US US344143A patent/US3350456A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
GB947112A (en) | 1964-01-22 |
US3350456A (en) | 1967-10-31 |
DE1296625B (de) | 1969-06-04 |
CH392495A (de) | 1965-05-31 |
NL122629C (en, 2012) | |
BE605777A (fr) | 1961-11-03 |
SE303130B (en, 2012) | 1968-08-19 |
NL259810A (en, 2012) |
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