CN1530357A - Method for catalytic conversion of alkyl cyclohexanol and alkyl cyclohexanone from air oxidized alkyl cyclohexane - Google Patents
Method for catalytic conversion of alkyl cyclohexanol and alkyl cyclohexanone from air oxidized alkyl cyclohexane Download PDFInfo
- Publication number
- CN1530357A CN1530357A CNA031181708A CN03118170A CN1530357A CN 1530357 A CN1530357 A CN 1530357A CN A031181708 A CNA031181708 A CN A031181708A CN 03118170 A CN03118170 A CN 03118170A CN 1530357 A CN1530357 A CN 1530357A
- Authority
- CN
- China
- Prior art keywords
- alkyl
- cyclohexane
- metalloporphyrin
- general formula
- cyclohexanol
- 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.)
- Granted
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process for selectively oxidizing alkyl cyclohexane by air under the catalysis of mu-oxygen bimetal porphyrin, single-metal porphyrin, or their solid carried substance to become alkyl cyclohexanol and alkyl cyclohexanone is disclosed. Said alkyl cyclohexane may be methyl cyclohexane, ethyl cyclohexane, isopropyl cyclohexane, etc. Its advantages are low cost, high catalytic performance, low reaction temp (less than 200 deg.C) and high transform rate.
Description
Technical field:
The present invention relates to the method that the catalytic air oxidation alkyl cyclohexane is alkyl cyclohexanol and alkyl cyclohexanone
Background technology
Alkyl cyclohexanol and alkyl cyclohexanone are owing to having the better fat-soluble important intermediate that is widely used in medicine, agricultural chemicals and fine chemistry industry than hexalin and pimelinketone.At present, industrial alkyl cyclohexanol is mainly by corresponding alkylphenol hydrogenation preparing, and alkyl cyclohexanone then is to be prepared through nucleophilic addition(Adn) through nucleophilic substitution or by cyclonene and alkyl copper lithium reagent by pimelinketone and halohydrocarbon.WO0214255 discloses the method for methylphenol hydrogenation preparing methyl-cyclohexanol, and CH595309 discloses the method for the direct hydrogenation preparing methylcyclohexanone of methylphenol.These methods that prepare alkyl cyclohexanol and alkyl cyclohexanone all adopt expensive pimelinketone or alkylphenol to make raw material, directly do not appear in the newspapers through the method that atmospheric oxidation prepares alkyl cyclohexanol and alkyl cyclohexanone and use low-cost alkyl cyclohexane to make raw material.
Summary of the invention:
The purpose of this invention is to provide a kind of synthetic low price, the oxide side chain that the catalyzed reaction temperature is low, can effectively control alkyl cyclohexane and product deep oxidation, alkyl cyclohexanol and alkyl cyclohexanone yield be big, and can pass through the CONTROL PROCESS condition, selectivity obtain different alcohol ketone ratios product a kind of efficiently, highly selective catalytic air oxidation alkyl cyclohexane becomes the novel method of alkyl cyclohexanol and alkyl cyclohexanone.
Technical scheme of the present invention is: feeding under the 1-15atm air conditions, control reaction temperature is 80-200 ℃, select for use by one or more or above-mentioned metalloporphyrin of general formula (I) or μ (II)-oxygen bimetallic porphyrin and monometallic porphyrin and inorganic and organic polymer and make catalyzer separately by the supported metalloporphyrin that physics or chemical process constitute, catalyst concn is 1-50PPM, and the catalytic air oxidation alkyl cyclohexane is alkyl cyclohexanol and alkyl cyclohexanone.
Described alkyl cyclohexane can be methylcyclohexane, ethylcyclohexane, normenthane, 1,2-dimethyl cyclohexane, 1,3-dimethyl cyclohexane, 1,4-dimethyl cyclohexane, isopropyl methyl hexanaphthene, 1,2,3-trimethyl-cyclohexane, 1,2,4-trimethyl-cyclohexane, 1,3, the 5-trimethyl-cyclohexane.
Technical scheme of the present invention can also be to feed under the 1-15atm air conditions, control reaction temperature is 80-200 ℃, select for use by general formula (I) or (II) metalloporphyrin or their immobilized thing as Primary Catalysts, with transition metal salt or oxide compound as co-catalyst, Primary Catalysts concentration is 1-50PPM, and the mol ratio of Primary Catalysts and co-catalyst is 1: the realization of getting off of the condition of 3-5.
Described μ-oxygen bimetallic porphyrin and monometallic porphyrin are following structural formula:
General formula (I)
General formula (II)
Atoms metal M in the above-mentioned metal porphyrins structure, M
1, M
2Can be transition metal atoms or lanthanide series metal atom; Substituent R on the phenyl ring
1, R
2, R
3Can be hydrogen, alkyl, alkoxyl group, hydroxyl, halogen, amido, amino, glycosyl replaces glycosyl and cyclodextrin.Dentate X can be an acetate, methyl ethyl diketone, halogen.
Catalyzer can be one or more of above-mentioned metalloporphyrin in the alkyl cyclohexane oxidizing process of the present invention.Also can be above-mentioned metalloporphyrin and supported metalloporphyrin inorganic and that organic polymer constitutes by physics or chemical process.
The carrier that constitutes the supported metalloporphyrin catalyzer with above-mentioned metalloporphyrin has: silica gel, molecular sieve, aluminum oxide, zeolite, sepiolite, porous ceramics, polyvinyl chloride, polyvinyl chloride, polystyrene etc.
Described transition metal salt or oxide compound as co-catalyst have: Cu, Zn, Fe, Co, Mn, Cr, Ni etc.These metal-salts or oxide compound can obviously improve the catalytic performance of metalloporphyrin to atmospheric oxidation alkyl hexamethylene hydrocarbon.
The present invention adopts low-cost alkyl cyclohexane to make raw material directly to prepare alkyl cyclohexanol and alkyl cyclohexanone through atmospheric oxidation and replace and make raw material with expensive pimelinketone or alkylphenol, thereby greatly reduce production cost, the results showed that μ-oxygen bimetallic porphyrin becomes the reaction of alkyl cyclohexanol and alkyl cyclohexanone to have good catalytic performance with the monometallic porphyrin to the atmospheric oxidation alkyl cyclohexane.With the variation of catalysis of metalloporphyrin agent composition and temperature of reaction, the alkyl cyclohexane transformation efficiency is between 15-25%.Because temperature of reaction is lower than 200 ℃, has effectively controlled the deep oxidation of alkyl cyclohexane, the total recovery of product alcohol and ketone can be greater than 90%.
Embodiment
Embodiment 1:
3mg had the metalloporphyrin of general formula (I), R
1=R
2=R
3=CH
3, M=Mn adds in the 400ml methylcyclohexane, feeds the 6atm air.130 ℃ of following reaction stirred 4 hours, the methylcyclohexane transformation efficiency was 18.2%, pure and mild ketone yield 95% in the reaction product.
Embodiment 2:
1mg had the metalloporphyrin of general formula (II), R
1=R
2=R
3=Cl, M
1=M
2=Fe adds 500ml 1, in the 4-dimethyl cyclohexane, feeds the 8atm air.160 ℃ of following reaction stirred 4 hours, 1,4-methylcyclohexane transformation efficiency is 15.5%, pure and mild ketone yield 92% in the reaction product.
Embodiment 3:
4mg had the metalloporphyrin of general formula (I), R
1=R
2=R
3=Cl, M=Fe and 15mg CoCl
2Add in the 500ml methylcyclohexane, feed the 10atm air.140 ℃ of following reaction stirred 3 hours, the methylcyclohexane transformation efficiency was 22.5%, pure and mild ketone yield 86% in the reaction product.
Embodiment 4:
4mg had the metalloporphyrin of general formula (II), R
1=R
2=R
3=Cl, M=Fe adds in the 500ml methylcyclohexane, feeds the 8atm air.90 ℃ of following reaction stirred 5 hours, the methylcyclohexane transformation efficiency was 18%, pure and mild ketone yield 90% in the reaction product.
Embodiment 5:
6mg had the metalloporphyrin of general formula (II), R
1=R
2=R
3=Cl, M=Fe adds in the 500ml methylcyclohexane, feeds the 11atm air.120 ℃ of following reaction stirred 1.5 hours, the methylcyclohexane transformation efficiency was 19%, pure and mild ketone yield 89% in the reaction product.
Embodiment 6:
3mg had the metalloporphyrin of general formula (I), R
1=R
2=R
3=Cl, M=Co adds in the 500ml methylcyclohexane, feeds the 10atm air.130 ℃ of following reaction stirred 2 hours, the methylcyclohexane transformation efficiency was 21%, pure and mild ketone yield 93% in the reaction product.
Embodiment 7:
2mg had the metalloporphyrin of general formula (I), R
1=R
2=R
3=Cl, M=Co adds 500ml 1, in the 3-dimethyl cyclohexane, feeds the 6atm air.180 ℃ of following reaction stirred 3 hours, 1,3-dimethyl cyclohexane transformation efficiency is 21%, pure and mild ketone yield 93% in the reaction product.
Embodiment 8:
4mg had the metalloporphyrin of general formula (I), R
1=R
2=R
3=Cl, M=Mn adds 500ml 1,3, in the 5-trimethyl-cyclohexane, feeds the 14atm air.110 ℃ of following reaction stirred 1 hour, 1,3,5-trimethyl-cyclohexane transformation efficiency is 23%, pure and mild ketone yield 90% in the reaction product.
Claims (5)
1, a kind of catalytic air oxidation alkyl cyclohexane is that alkyl cyclohexanol and alkyl cyclohexanone method is characterized in that feeding under the 1-15atm air conditions, control reaction temperature is 80-200 ℃, select for use by one or more or above-mentioned metalloporphyrin of general formula (I) or μ (II)-oxygen bimetallic porphyrin and monometallic porphyrin and inorganic and organic polymer and make catalyzer separately by the supported metalloporphyrin that physics or chemical process constitute, catalyst concn is 1-50PPM
General formula (I)
General formula (II)
Atoms metal M in the said structure, M
1, M
2Can be transition metal atoms or lanthanide series metal atom; Substituent R on the phenyl ring
1, R
2, R
3Can be hydrogen, alkyl, alkoxyl group, hydroxyl, halogen, amido, amino, glycosyl replaces glycosyl and cyclodextrin.Dentate X can be an acetate, methyl ethyl diketone, halogen.
2, a kind of catalytic air oxidation alkyl cyclohexane is alkyl cyclohexanol and alkyl cyclohexanone method, it is characterized in that feeding the 1-15atm air, temperature of reaction is 50-200 ℃, select that one or more or above-mentioned metalloporphyrin and the inorganic and organic polymer of metalloporphyrin are made Primary Catalysts by the supported metalloporphyrin that physics or chemical process constitute by general formula (I) or (II) for use, the consumption of Primary Catalysts is 1-50PPM, make co-catalyst with transition metal salt or oxide compound, the mol ratio of Primary Catalysts and co-catalyst is 1: 3-5.
3, according to claim 1 or 2 described methods, it is characterized in that described alkyl cyclohexane can be methylcyclohexane, ethylcyclohexane, normenthane, 1,2-dimethyl cyclohexane, 1,3-dimethyl cyclohexane, 1,4-dimethyl cyclohexane, isopropyl methyl hexanaphthene, 1,2,3-trimethyl-cyclohexane, 1,2,4-trimethyl-cyclohexane, 1,3, the 5-trimethyl-cyclohexane.
4. according to claim 1 or 2 described methods, it is characterized in that: metalloporphyrin can constitute supported metalloporphyrin with following carrier: silica gel, molecular sieve, aluminum oxide, zeolite, sepiolite, porous ceramics, polyvinyl chloride, polyvinyl chloride, polystyrene, chitin, Mierocrystalline cellulose.
5,, it is characterized in that described metal-salt or oxide compound can be the salt or the oxide compound of following metal: Cu, Zn, Fe, Co, Mn, Cr, Ni according to claim 1 or 2 described methods.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB031181708A CN100402477C (en) | 2003-03-14 | 2003-03-14 | Method for catalytic conversion of alkyl cyclohexanol and alkyl cyclohexanone from air oxidized alkyl cyclohexane |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB031181708A CN100402477C (en) | 2003-03-14 | 2003-03-14 | Method for catalytic conversion of alkyl cyclohexanol and alkyl cyclohexanone from air oxidized alkyl cyclohexane |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1530357A true CN1530357A (en) | 2004-09-22 |
| CN100402477C CN100402477C (en) | 2008-07-16 |
Family
ID=34284858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB031181708A Expired - Fee Related CN100402477C (en) | 2003-03-14 | 2003-03-14 | Method for catalytic conversion of alkyl cyclohexanol and alkyl cyclohexanone from air oxidized alkyl cyclohexane |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100402477C (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1317247C (en) * | 2004-12-09 | 2007-05-23 | 中国石化集团巴陵石油化工有限责任公司 | Method of obtaining high purity cyclohexanol from cyclohexane oxidation product |
| CN100393680C (en) * | 2006-05-22 | 2008-06-11 | 湖南大学 | Technology and apparatus for preparing cyclohexanol, cyclohexanone and adipic acid by cyclohexane |
| CN101747204A (en) * | 2010-01-29 | 2010-06-23 | 北京工业大学 | Method for preparing p-nitroacetophenone by biomimetic catalytic oxidation of p-nitroethylbenzene with oxygen |
| CN101774925A (en) * | 2010-01-29 | 2010-07-14 | 北京工业大学 | Method for preparing o-nitroacetophenone by oxidizing o-nitroethylbenzene through biomimetic-catalysis oxygen |
| CN101838189A (en) * | 2007-07-06 | 2010-09-22 | 南京理工大学 | Preparation method of metal deuteroporphyrin compound and application method thereof |
| CN102343281A (en) * | 2011-08-05 | 2012-02-08 | 红河学院 | Catalyst for catalyzing and oxidizing cyclohexane into cyclohexanone under liquid phase condition |
| CN101367709B (en) * | 2008-09-22 | 2012-04-25 | 广西大学 | Method for catalysis of atmospheric oxidation cyclohexane with ultra-fine A100H-supported metalloporphyrin |
| CN101747166B (en) * | 2010-01-29 | 2013-04-03 | 北京工业大学 | Method for preparing m-ethylacetophenone by biomimetic catalytic oxidation of m-diethylbenzene with oxygen |
| CN103055939A (en) * | 2012-12-11 | 2013-04-24 | 广西大学 | Preparation method for porous biomimetic catalytic material and application thereof |
| CN104098434A (en) * | 2014-08-04 | 2014-10-15 | 中国林业科学研究院林产化学工业研究所 | 1-isopropyl-4-methylcyclohexane product and preparation method thereof |
| JP2016500666A (en) * | 2012-10-05 | 2016-01-14 | ヴェ マン フィユＶ． Ｍａｎｅ Ｆｉｌｓ | Process for the synthesis of cyclohexenone and its use in perfumery production |
| CN110526801A (en) * | 2019-08-28 | 2019-12-03 | 浙江工业大学 | Method for oxidizing cycloalkane by cobalt (II) porphyrin/copper (II) porphyrin salt concerted catalysis |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1116258C (en) * | 2000-01-17 | 2003-07-30 | 郭灿城 | Catalytic oxidation process of alkane and naphthene hydrocarbon |
-
2003
- 2003-03-14 CN CNB031181708A patent/CN100402477C/en not_active Expired - Fee Related
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1317247C (en) * | 2004-12-09 | 2007-05-23 | 中国石化集团巴陵石油化工有限责任公司 | Method of obtaining high purity cyclohexanol from cyclohexane oxidation product |
| CN100393680C (en) * | 2006-05-22 | 2008-06-11 | 湖南大学 | Technology and apparatus for preparing cyclohexanol, cyclohexanone and adipic acid by cyclohexane |
| CN101838189A (en) * | 2007-07-06 | 2010-09-22 | 南京理工大学 | Preparation method of metal deuteroporphyrin compound and application method thereof |
| CN101367709B (en) * | 2008-09-22 | 2012-04-25 | 广西大学 | Method for catalysis of atmospheric oxidation cyclohexane with ultra-fine A100H-supported metalloporphyrin |
| CN101747166B (en) * | 2010-01-29 | 2013-04-03 | 北京工业大学 | Method for preparing m-ethylacetophenone by biomimetic catalytic oxidation of m-diethylbenzene with oxygen |
| CN101774925A (en) * | 2010-01-29 | 2010-07-14 | 北京工业大学 | Method for preparing o-nitroacetophenone by oxidizing o-nitroethylbenzene through biomimetic-catalysis oxygen |
| CN101747204B (en) * | 2010-01-29 | 2012-12-05 | 北京工业大学 | Method for preparing p-nitroacetophenone by biomimetic catalytic oxidation of p-nitroethylbenzene with oxygen |
| CN101747204A (en) * | 2010-01-29 | 2010-06-23 | 北京工业大学 | Method for preparing p-nitroacetophenone by biomimetic catalytic oxidation of p-nitroethylbenzene with oxygen |
| CN101774925B (en) * | 2010-01-29 | 2013-05-08 | 北京工业大学 | Method for preparing o-nitroacetophenone by oxidizing o-nitroethylbenzene through biomimetic-catalysis oxygen |
| CN102343281A (en) * | 2011-08-05 | 2012-02-08 | 红河学院 | Catalyst for catalyzing and oxidizing cyclohexane into cyclohexanone under liquid phase condition |
| JP2016500666A (en) * | 2012-10-05 | 2016-01-14 | ヴェ マン フィユＶ． Ｍａｎｅ Ｆｉｌｓ | Process for the synthesis of cyclohexenone and its use in perfumery production |
| JP2018104442A (en) * | 2012-10-05 | 2018-07-05 | ヴェ マン フィユＶ． Ｍａｎｅ Ｆｉｌｓ | Method for synthesising cyclohexenones and use of the same in perfume production |
| CN103055939A (en) * | 2012-12-11 | 2013-04-24 | 广西大学 | Preparation method for porous biomimetic catalytic material and application thereof |
| CN103055939B (en) * | 2012-12-11 | 2014-11-26 | 广西大学 | Preparation method for porous biomimetic catalytic material and application thereof |
| CN104098434A (en) * | 2014-08-04 | 2014-10-15 | 中国林业科学研究院林产化学工业研究所 | 1-isopropyl-4-methylcyclohexane product and preparation method thereof |
| CN104098434B (en) * | 2014-08-04 | 2016-02-24 | 中国林业科学研究院林产化学工业研究所 | A kind of to alkanol product and preparation method thereof in the Meng |
| CN110526801A (en) * | 2019-08-28 | 2019-12-03 | 浙江工业大学 | Method for oxidizing cycloalkane by cobalt (II) porphyrin/copper (II) porphyrin salt concerted catalysis |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100402477C (en) | 2008-07-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1530357A (en) | Method for catalytic conversion of alkyl cyclohexanol and alkyl cyclohexanone from air oxidized alkyl cyclohexane | |
| CN110102350B (en) | Catalyst for oxidative synthesis of 2, 5-furandicarboxylic acid and preparation method and application thereof | |
| CN1199922C (en) | Oxidation method | |
| US8410315B2 (en) | Method for producing olefinically unsaturated carbonyl compounds by oxidative dehydrogenation of alcohols | |
| CN107253937B (en) | A kind of synthetic method of gamma-valerolactone | |
| CN1191218C (en) | Method for atmospheric catalytic oxidation of cyclohexane by metalloporphyrin | |
| CN102070382B (en) | Method for preparing benzaldehyde or substituted benzaldehyde by catalytically oxidizing methylbenzene or substituted methylbenzene | |
| US20100130758A1 (en) | Method for producing carbonyl compound | |
| CN1273443C (en) | Method for preparing oxime by using ammonium salt or substituted ammonium salt through cocatalysis | |
| CN1218922C (en) | Method of preparing adipic acid by air-oxidating hexacarbocyclic compound | |
| CN114939438B (en) | Method for selective hydrogenation of olefinic unsaturated carbonyl compound and catalyst thereof | |
| CN1283602C (en) | Method of catalyzed oxidation of olefin to produce enol, ketenes and epoxy compound | |
| CN1156421C (en) | Process for preparing methyl benzaldehyde, methyl methanol and methyl benzoic acid by selectiveoxidizing dimethylbenzene | |
| CN1414937A (en) | Method for producing alcohol/ketone mixtures | |
| CN100494134C (en) | Process for preparing aldehyde and alcohol by selectively catalytic air oxidation for toluene and substituted toluene | |
| CN1116258C (en) | Catalytic oxidation process of alkane and naphthene hydrocarbon | |
| CN1269785C (en) | Process for preparing aldehyde ketone and acid by oxidation of olefin | |
| CN1740129A (en) | Prepn process of hydroquinone and phenol | |
| CN1310865C (en) | Method of catalyzing oxidation of aromatic methyl benzene with air to prepare aromatic carboxylic acid | |
| CN101225067B (en) | Method for preparing hydroperoxidation p-menthane by catalytic air oxidation p-menthane | |
| Kusy et al. | Recent advances in the application of nanoparticles in the selective reduction of carbon–carbon double bonds | |
| CN1629125A (en) | Method for catalytic oxidation preparation of methyl formate from methanol | |
| CN100445255C (en) | Method for catalytic hydrogenation of six carbocyclic compound by schiff bases-porphyrin metallic compound | |
| CN1491930A (en) | Synthetic process for p-methoxy benzaldehyde | |
| CN115385783A (en) | Method for synthesizing p-hydroxybenzaldehyde by catalytic oxidation of p-cresol with metal phthalocyanine |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080716 Termination date: 20130314 |