CN109369327A - A kind of cycloalkane catalysis oxidation new method that nickel-porphyrin promotes - Google Patents

A kind of cycloalkane catalysis oxidation new method that nickel-porphyrin promotes Download PDF

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CN109369327A
CN109369327A CN201811467575.9A CN201811467575A CN109369327A CN 109369327 A CN109369327 A CN 109369327A CN 201811467575 A CN201811467575 A CN 201811467575A CN 109369327 A CN109369327 A CN 109369327A
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tetra
porphyrin
cycloalkane
porphyrins
nickel
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沈海民
孙静
佘远斌
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Zhejiang University of Technology ZJUT
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Zhejiang University of Technology ZJUT
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
    • 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
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1825—Ligands comprising condensed ring systems, e.g. acridine, carbazole
    • B01J31/183—Ligands comprising condensed ring systems, e.g. acridine, carbazole with more than one complexing nitrogen atom, e.g. phenanthroline
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/48—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
    • C07C29/50—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only
    • 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
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties

Abstract

A kind of method for the cycloalkane catalysis oxidation that nickel-porphyrin promotes, described method includes following steps: cycloalkane, major catalyst, co-catalyst being mixed, in 100~160 DEG C of temperature, O22~48h is reacted under conditions of 0.8~2MPa of pressure, reaction solution is post-processed later, obtains oxidation product alkyl acid, cycloalkyl alcohol, naphthenic one；Cycloalkane catalysis oxidation new method oxidation product selectivity of the present invention is high, and reaction temperature is low, and catalyst amount is few, and with O2It is environmentally protective for oxidant, can realize the catalysis oxidation of cycloalkane with high selectivity, the cycloalkane catalysis oxidation new method also have it is easy to operate, without using the advantages such as organic solvent.

Description

A kind of cycloalkane catalysis oxidation new method that nickel-porphyrin promotes
(1) technical field
The present invention relates to the cycloalkane catalysis oxidation new methods that a kind of nickel-porphyrin promotes, and belong to catalysis organic synthesis field.
(2) background technique
Cycloalkane catalysis oxidation is an important chemical industry conversion process, and oxidation product cycloalkyl alcohol, naphthenic one are not It is only important chemical intermediate, further oxidation can also prepare alkyl acid, and alkyl acid is to prepare various macromolecules The important as precursors of material.Alkyl acid also can be generated in cycloalkanes oxidation process simultaneously, is directly used in various high molecular materials Preparation.As the primary product cyclohexanol and cyclohexanone of catalytic oxidation of cyclohexane further aoxidize available production nylon -66 and The important as precursors adipic acid of nylon-6, the market demand it is very big (Angew.Chem.Int.Edit., 2016,55:12873； J.Am.Chem.Soc.,2016,138:2426；Ind.Eng.Chem.Res.,2015,54:2425；Appl.Surf.Sci., 2017,402:436.).But cycloalkane catalysis oxidation is low in the prevalence of the substrate transformation rate at present, selectivity of product is poor, receives The low shortcoming of rate, especially with clean O2For the oxidation process of oxidant, above-mentioned shortcoming is become apparent, especially Selectivity of product is low.It traces sth. to its source, cycloalkane catalytic oxidation process oxidation product is selectively low mainly since oxidation process is raw At intermediate product cycloalkylhydroperoxide mainly pass through thermal decomposition and converted to cycloalkyl alcohol, naphthenic one and alkyl acid, it is difficult With control.Therefore, the decomposition and inversion for regulating and controlling and promoting cycloalkylhydroperoxide during cycloalkanes oxidation is urged cycloalkane is improved The selectivity for changing oxidation has great importance, and industrial application value is very big.
Model compound of the metalloporphyrin as cytochrome P-450 is widely used in all kinds of organic syntheses of bionic catalysis Reaction, especially oxidation reaction (New J.Chem., 2017,41:8214；Catal.Commun.,2017,99:100；New J.Chem.,2017,41:7987；Chem.Lett., 2017,46:1311), few, high catalytic efficiency, knot with catalyst amount Structure is easy to adjust, bio-compatibility is good, the advantages such as environmentally protective.The present invention is respectively with Co (II) porphyrin, Mn (II) porphyrin or Fe (II) porphyrin be major catalyst, using Ni (II) porphyrin be co-catalyst regulate and control and promotion cycloalkanes oxidation during naphthenic base peroxide The decomposition and inversion for changing hydrogen, significantly improves the selectivity of cyclopentanone, cyclohexanol, cycloheptanone and cyclooctanone.Therefore, the present invention is with nickel Porphyrin promotes cycloalkane catalysis oxidation, improves the selectivity of oxidation product, has important industrial application value and social effect, And it is environmentally protective, meet current chemical industry sexual development compatible with ecological environment, the current demand of sustainable development.
(3) summary of the invention
The purpose of the present invention is to provide the cycloalkane catalysis oxidation new methods that a kind of nickel-porphyrin promotes.This method is with O2For Oxidant, respectively using Co (II) porphyrin, Mn (II) porphyrin or Fe (II) porphyrin as major catalyst, using Ni (II) porphyrin as co-catalysis Agent is realized under condition of no solvent.
Technical scheme is as follows:
A kind of method for the cycloalkane catalysis oxidation that nickel-porphyrin promotes, described method includes following steps:
Cycloalkane, major catalyst, co-catalyst are mixed, in temperature 100~160 DEG C of (preferably 110~120 DEG C), O2Pressure 2~48h (preferably 4~10h) is reacted under conditions of 0.8~2MPa of power (preferably 1~1.6MPa), after reaction solution carries out later Reason, obtains oxidation product alkyl acid, cycloalkyl alcohol, naphthenic one；
The cycloalkane is pentamethylene, hexamethylene, cycloheptane, cyclooctane or cyclononane；
Mixed liquor is obtained after the cycloalkane, major catalyst, co-catalyst mixing, major catalyst concentration in the mixed liquor For 10~60ppm (preferably 20~50ppm)；
The major catalyst, co-catalyst mass ratio be 1:0.1~10, preferably 1:0.2~5；
The major catalyst is selected from 5,10,15,20- tetra- (p- chlorphenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (p- chlorine Phenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (p- chlorphenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (m- chlorphenyl) porphyrins Cobalt (II), 5,10,15,20- tetra- (m- chlorphenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (m- chlorphenyl) Manganese Porphyrins (II), 5, 10,15,20- tetra- (o- chlorphenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (o- chlorphenyl) PORPHYRIN IRONs (II), 5,10,15,20- Four (o- chlorphenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (2,6- dichlorophenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (2, 6- dichlorophenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (2,6- dichlorophenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (3, 5- dichlorophenyl) Cobalt Porphyrin (II), 5,10,15,20- tetra- (3,5- dichlorophenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (3, 5- dichlorophenyl) Manganese Porphyrin (II), 5,10,15,20- tetra- (2,4- dichlorophenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (2, 4- dichlorophenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (2,4- dichlorophenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (p- Fluorophenyl) Cobalt Porphyrin (II), 5,10,15,20- tetra- (p- fluorophenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (p- fluorophenyl) porphins Quinoline manganese (II), 5,10,15,20- tetra- (m- fluorophenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (m- fluorophenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (m- fluorophenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (o- fluorophenyl) Cobalt Porphyrins (II), 5,10,15, Any one in 20- tetra- (o- fluorophenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (o- fluorophenyl) Manganese Porphyrins (II), preferably 5,10,15,20- tetra- (p- chlorphenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (m- chlorphenyl) Cobalt Porphyrins (II) or 5,10,15, 20- tetra- (o- chlorphenyl) Cobalt Porphyrin (II)；
The co-catalyst is selected from 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (m- chlorine Phenyl) Porphyrin Nickel (II), 5,10,15,20- tetra- (o- chlorphenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (2,6- dichlorophenyls) Porphyrin Nickel (II), 5,10,15,20- tetra- (3,5- dichlorophenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (2,4- dichlorophenyls) Porphyrin Nickel (II), 5,10,15,20- tetra- (p- fluorophenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (m- fluorophenyl) Porphyrin Nickels (II), any one in 5,10,15,20- tetra- (o- fluorophenyl) Porphyrin Nickels (II), preferably 5,10,15,20- tetra- (p- chlorobenzenes Base) Porphyrin Nickel (II), 5,10,15,20- tetra- (m- chlorphenyl) Porphyrin Nickels (II) or 5,10,15,20- tetra- (o- chlorphenyl) porphyrins Nickel (II)；
Specifically, the method for the post-processing are as follows: after reaction, be cooled to room temperature (20~30 DEG C), mistake to reaction solution Filter, filter cake is washed with cycloalkane, and is dried in vacuo at 60 DEG C, and alkyl acid is obtained；Filtrate carries out rectifying or rectification under vacuum (this Field routine techniques), naphthenic one, cycloalkyl alcohol (while unreacted cycloalkane is recycled in rectifying) are collected respectively.
The beneficial effects are mainly reflected as follows: the cycloalkane catalysis oxidation new method oxidation product selectivity being related to Height, reaction temperature is low, and catalyst amount is few, and with O2It is environmentally protective for oxidant, cycloalkane can be realized with high selectivity Catalysis oxidation.The cycloalkane catalysis oxidation new method also have it is easy to operate, without using the advantages such as organic solvent.
(4) specific embodiment
The present invention is described further combined with specific embodiments below, but protection scope of the present invention is not limited in This.
Embodiment 1
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) is dissolved in 50.0g hexamethylene, close autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h is stirred to react under pressure, stirring is cooled to room temperature in ice-water bath.Autoclave is opened, gained is anti- Mixture is answered to filter, obtained solid is washed through 3 × 5mL hexamethylene, is dried in vacuo at 60 DEG C, as adipic acid, and HPLC analysis is received Rate 0.32%, filtrate GC analyze to obtain cyclohexanol yield 1.45%, cyclohexanone yield 1.49%.
Embodiment 2
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Porphyrin Nickel (II) is dissolved in 50.0g hexamethylene, close autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h is stirred to react under pressure, stirring is cooled to room temperature in ice-water bath.Autoclave is opened, gained is anti- Mixture HPLC is answered, adipic acid, cyclohexanol and cyclohexanone is not detected in GC analysis.
Embodiment 3
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.18%, and filtrate GC analyzes to obtain cyclohexanol yield 1.84%, Cyclohexanone yield 1.63%.
Embodiment 4
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 0.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.11%, and filtrate GC analyzes to obtain cyclohexanol yield 1.83%, Cyclohexanone yield 1.67%.
Embodiment 5
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 0.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.14%, and filtrate GC analyzes to obtain cyclohexanol yield 1.40%, Cyclohexanone yield 1.01%.
Embodiment 6
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 3.0mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.18%, and filtrate GC analyzes to obtain cyclohexanol yield 2.13%, Cyclohexanone yield 2.36%.
Embodiment 7
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 3.0mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.12%, and filtrate GC analyzes to obtain cyclohexanol yield 2.13%, Cyclohexanone yield 1.46%.
Embodiment 8
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 2.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 2.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.26%, and filtrate GC analyzes to obtain cyclohexanol yield 2.23%, Cyclohexanone yield 1.98%.
Embodiment 9
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 0.8MPa, in 120 DEG C, 0.8MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.06%, and filtrate GC analyzes to obtain cyclohexanol yield 0.79%, Cyclohexanone yield 0.13%.
Embodiment 10
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 2.0MPa, in 120 DEG C, 2.0MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.49%, and filtrate GC analyzes to obtain cyclohexanol yield 2.35%, Cyclohexanone yield 2.64%.
Embodiment 11
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.6MPa, in 120 DEG C, 1.6MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.11%, and filtrate GC analyzes to obtain cyclohexanol yield 2.35%, Cyclohexanone yield 1.62%.
Embodiment 12
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 100 DEG C, is passed through O2To 1.4MPa, in 100 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.02%, and filtrate GC analyzes to obtain cyclohexanol yield 0.16%, Cyclohexanone yield 0.20%.
Embodiment 13
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 160 DEG C, is passed through O2To 1.4MPa, in 160 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 2.35%, and filtrate GC analyzes to obtain cyclohexanol yield 0.92%, Cyclohexanone yield 1.58%.
Embodiment 14
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O22.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.02%, and filtrate GC analyzes to obtain cyclohexanol yield 0.16%, Cyclohexanone yield 0.08%.
Embodiment 15
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O248.0h, ice are stirred to react under pressure Stirred in water bath is cooled to room temperature.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 1.26%, and filtrate GC analyzes to obtain cyclohexanol yield 2.84%, Cyclohexanone yield 1.64%.
Embodiment 16
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g pentamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL pentamethylene It washing, is dried in vacuo at 60 DEG C, as glutaric acid, HPLC analyzes yield 1.65%, and filtrate GC analyzes to obtain cyclopentanol yield 0.23%, Cyclopentanone yield 1.86%.
Embodiment 17
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g cyclooctane, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL cyclooctane It washing, is dried in vacuo at 60 DEG C, as suberic acid, HPLC analyzes yield 0.02%, and filtrate GC analyzes to obtain Lotka-Volterra circle system yield 6.35%, Cyclooctanone yield 7.92%.
Embodiment 18
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (m- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (o- chlorphenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, close Autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O28.0h, ice water are stirred to react under pressure Stirring is cooled to room temperature in bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is washed through 3 × 5mL hexamethylene It washing, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.18%, and filtrate GC analyzes to obtain cyclohexanol yield 1.94%, Cyclohexanone yield 1.54%.
Embodiment 19
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 1.5mg 5,10,15,20- tetra- (3,5- bis- Chlorphenyl) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (p- fluorophenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, Close autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O2It is stirred to react 8.0h under pressure, Stirring is cooled to room temperature in ice-water bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is through 3 × 5mL hexamethylene It washs, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.11%, and filtrate GC analyzes to obtain cyclohexanol yield 1.85%, cyclohexanone yield 1.62%.
Embodiment 20
In the stainless steel autoclave that 100mL has tetrafluoroethene liner, by 5,10,15,20- tetra- (p- chlorobenzene of 1.5mg Base) Cobalt Porphyrin (II) and 5,10,15,20- tetra- (3,5- dichlorophenyl) Porphyrin Nickel (II) of 1.5mg be dissolved in 50.0g hexamethylene, Close autoclave.Stirring is warming up to 120 DEG C, is passed through O2To 1.4MPa, in 120 DEG C, 1.4MPa O2It is stirred to react 8.0h under pressure, Stirring is cooled to room temperature in ice-water bath.Autoclave is opened, gained reaction mixture is filtered, obtained solid is through 3 × 5mL hexamethylene It washs, is dried in vacuo at 60 DEG C, as adipic acid, HPLC analyzes yield 0.62%, and filtrate GC analyzes to obtain cyclohexanol yield 2.35%, cyclohexanone yield 1.68%.

Claims (7)

1. a kind of method for the cycloalkane catalysis oxidation that nickel-porphyrin promotes, which is characterized in that described method includes following steps:
Cycloalkane, major catalyst, co-catalyst are mixed, in 100~160 DEG C of temperature, O2It is anti-under conditions of 0.8~2MPa of pressure 2~48h is answered, reaction solution is post-processed later, obtains oxidation product alkyl acid, cycloalkyl alcohol, naphthenic one；
The cycloalkane is pentamethylene, hexamethylene, cycloheptane, cyclooctane or cyclononane；
Mixed liquor is obtained after the cycloalkane, major catalyst, co-catalyst mixing, major catalyst concentration is 10 in the mixed liquor ~60ppm；
The major catalyst, co-catalyst mass ratio be 1:0.1~10；
The major catalyst is selected from 5,10,15,20- tetra- (p- chlorphenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (p- chlorphenyls) PORPHYRIN IRON (II), 5,10,15,20- tetra- (p- chlorphenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (m- chlorphenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (m- chlorphenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (m- chlorphenyl) Manganese Porphyrins (II), 5, 10,15,20- tetra- (o- chlorphenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (o- chlorphenyl) PORPHYRIN IRONs (II), 5,10,15,20- Four (o- chlorphenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (2,6- dichlorophenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (2, 6- dichlorophenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (2,6- dichlorophenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (3, 5- dichlorophenyl) Cobalt Porphyrin (II), 5,10,15,20- tetra- (3,5- dichlorophenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (3, 5- dichlorophenyl) Manganese Porphyrin (II), 5,10,15,20- tetra- (2,4- dichlorophenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (2, 4- dichlorophenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (2,4- dichlorophenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (p- Fluorophenyl) Cobalt Porphyrin (II), 5,10,15,20- tetra- (p- fluorophenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (p- fluorophenyl) porphins Quinoline manganese (II), 5,10,15,20- tetra- (m- fluorophenyl) Cobalt Porphyrins (II), 5,10,15,20- tetra- (m- fluorophenyl) PORPHYRIN IRONs (II), 5,10,15,20- tetra- (m- fluorophenyl) Manganese Porphyrins (II), 5,10,15,20- tetra- (o- fluorophenyl) Cobalt Porphyrins (II), 5,10,15, Any one in 20- tetra- (o- fluorophenyl) PORPHYRIN IRON (II), 5,10,15,20- tetra- (o- fluorophenyl) Manganese Porphyrins (II)；
The co-catalyst is selected from 5,10,15,20- tetra- (p- chlorphenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (m- chlorphenyls) Porphyrin Nickel (II), 5,10,15,20- tetra- (o- chlorphenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (2,6- dichlorophenyl) porphyrins Nickel (II), 5,10,15,20- tetra- (3,5- dichlorophenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (2,4- dichlorophenyl) porphyrins Nickel (II), 5,10,15,20- tetra- (p- fluorophenyl) Porphyrin Nickels (II), 5,10,15,20- tetra- (m- fluorophenyl) Porphyrin Nickels (II), 5, Any one in 10,15,20- tetra- (o- fluorophenyl) Porphyrin Nickels (II).
2. the method for the cycloalkane catalysis oxidation that nickel-porphyrin as described in claim 1 promotes, which is characterized in that reaction temperature is 110~120 DEG C.
3. the method for the cycloalkane catalysis oxidation that nickel-porphyrin as described in claim 1 promotes, which is characterized in that O2Pressure be 1~ 1.6MPa。
4. the method for the cycloalkane catalysis oxidation that nickel-porphyrin as described in claim 1 promotes, which is characterized in that the reaction time is 4~10h.
5. the method for the cycloalkane catalysis oxidation that nickel-porphyrin as described in claim 1 promotes, which is characterized in that the mixed liquor Middle major catalyst concentration is 20~50ppm.
6. the method for the cycloalkane catalysis oxidation that nickel-porphyrin as described in claim 1 promotes, which is characterized in that the main catalytic Agent, co-catalyst mass ratio be 1:0.2~5.
7. the method for the cycloalkane catalysis oxidation that nickel-porphyrin as described in claim 1 promotes, which is characterized in that the post-processing Method are as follows: after reaction, be cooled to room temperature, filter to reaction solution, filter cake washs with cycloalkane, and vacuum is dry at 60 DEG C It is dry, obtain alkyl acid；Filtrate carries out rectifying or rectification under vacuum, collects naphthenic one, cycloalkyl alcohol respectively.
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CN110483222A (en) * 2019-08-28 2019-11-22 浙江工业大学 A kind of method of second benzene-like compounds selective oxidation
CN110560169A (en) * 2019-08-19 2019-12-13 浙江工业大学 Cycloparaffin catalytic oxidation method promoted by iron porphyrin
CN113649073A (en) * 2021-08-11 2021-11-16 浙江工业大学 Method for catalytic oxidation of cycloparaffin by metalloporphyrin bimetallic center 2D MOFs

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CN110560169A (en) * 2019-08-19 2019-12-13 浙江工业大学 Cycloparaffin catalytic oxidation method promoted by iron porphyrin
CN110483222A (en) * 2019-08-28 2019-11-22 浙江工业大学 A kind of method of second benzene-like compounds selective oxidation
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