Aerobic Oxidation Catalyzed by Mixed Addenda Heteropolyoxometarates
| Project/Area Number |
06453143
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Synthetic chemistry
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| Research Institution | Kansai University |
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Principal Investigator |
ISHII Yasutaka Kansai Univ., Fac.Eng., Professor, 工学部, 教授 (50067675)
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| Co-Investigator(Kenkyū-buntansha) |
NISHIYAMA Yutaka Kansai Univ., Fac.Eng., Lecturer, 工学部, 専任講師 (30180665)
HAMANAKA Sawako Kansai Univ., Fac.Eng., Professor, 工学部, 教授 (90067611)
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| Project Period (FY) |
1994 – 1995
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| Project Status |
Completed (Fiscal Year 1995)
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| Budget Amount *help |
¥4,600,000 (Direct Cost: ¥4,600,000)
Fiscal Year 1995: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1994: ¥3,400,000 (Direct Cost: ¥3,400,000)
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| Keywords | oxygen / oxidation / aerobic oxidation / heteropolyacids / N-hydroxyphthalimide / alkane / amine / catalyst / バナドモリブドリン酸 / 自動酸化 / 混合配位ヘテロポリ酸 |
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| Research Abstract |
Oxidations of variountaining vanadium and molybdenum were examined. In addition, the combination of Pd (II) with vanadomolybdophosphate (NPVMo) in the presence of hydroquinone was found to be an efficient catalytic system for the oxidation of alkenes with molecular oxygen. We have obtained the following results in this project.
1. Oxidation of various organic substrates with molecular oxygen by NPVMo
Vanadomolybdophosphate (NPVMo), which can be shown as (NH_4) _5H_6PV_4Mo_8O_<40>, catalyzed the oxidation of aromatic amines, benzyl alcohols and phenols to the corresponding imines, bezaldehydes and quinoes with molecular oxygen under relatively mild conditions.
2. Development of indirect oxidation using molecular oxygen as final oxidant
Hydroquinone was smoothly dehydrogenated with molecular oxygen to quinone by NPVMo. By combination of Pd (II) and this system, anew oxidation system has been developed. Thus, a variety of cycloalkenes such as cyclohexene underwent the acylation in acetic acid by Pd (II) /hydroquinone/NPVMo/O_2 system to form 3-acetoxy-1-cycloalkenes in quantitative yields. When ethyl acrylate and acrylonitrile was allowed to react in ehtanol by the use of this catalytic system, acetalization took place to form the corresponding acetals in good yields.
3. Oxidation by the use of N-hydroxyphthalimide as catalyst
N-Hydroxyphthalimide (NHPI) was found to catalyze the oxidation of benzylic compounds with molecular oxygen to give alcohols or ketones in fair yields. This catalytic oxidation was found to be a novel aerobic oxidation system. The oxidation of alkanes such as cyclohexane was achieved by NHPI in the presence of Co (acac) n (n=2 or 3). For example, cyclohexane was converted to cyclohexanone and adipic acid in fair yields. This method was extended to the aerobic oxidation of various organic substrates.
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Report
(3 results)
Research Products
(11 results)
