Aerobic oxidation behavior of α-ionone catalyzed by N-hydroxyphthalimide combined with acetylacetone cobalt(II)

Rui-ren Tang , Ya-ping Zhou , Nian-hua Gong , Yu Zhao

Journal of Central South University ›› 2008, Vol. 15 ›› Issue (4) : 474 -478.

PDF
Journal of Central South University ›› 2008, Vol. 15 ›› Issue (4) : 474 -478. DOI: 10.1007/s11771-008-0089-5
Article

Aerobic oxidation behavior of α-ionone catalyzed by N-hydroxyphthalimide combined with acetylacetone cobalt(II)

Author information +
History +
PDF

Abstract

A practical catalytic method to oxidize α-ionone with molecular oxygen using N-hydroxyphthalimide(NHPI) combined with acetylacetone cobatt(II) (Co(acac)2) was developed, and the probable catalytic mechanism was proposed. The influences of the reaction conditions on conversion of α-ionone and the selectivity of the major product (5-keto-α-ionone) were investigated, and the technical parameters for 5-keto-α-ionone were optimized. The results show that the primary product is 5-keto-α-ionone, and by-products include epoxy-α-ionone, as well as rearrangement products 4-keto-β-ionone and epoxy-β-ionone, which are characterized by infrared spectra, proton nuclear magnetic resonance spectra, mass spectra and elemental analysis. The selectivity of 5-keto-α-ionone and the conversion of α-ionone are 55.0% and 97.0%, respectively, when 30%(molar fraction) NHPI, 1.0%(molar fraction) Co(acac)2 and no solvent are employed under O2 pressure of 1.0 MPa and the reaction temperature of 65 °C for 11 h. The procedure shows good reproducibility in the parallel experiments.

Keywords

catalytic oxidation / α-ionone / 5-keto-α-ionone / N-hydroxyphthalimide

Cite this article

Download citation ▾
Rui-ren Tang, Ya-ping Zhou, Nian-hua Gong, Yu Zhao. Aerobic oxidation behavior of α-ionone catalyzed by N-hydroxyphthalimide combined with acetylacetone cobalt(II). Journal of Central South University, 2008, 15(4): 474-478 DOI:10.1007/s11771-008-0089-5

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

PunniyamurthyT., VelusamyS., IqbalJ.. Recent advances in transition metal catalyzed oxidation of organic substrates with molecular oxygen [J]. Chemical Reviews, 2005, 105(6): 2329-2363

[2]

RajabiF., KarimiB.. Efficient aerobic oxidation of alcohols using a novel combination N-hydroxyphthalimide(NHPI) and a recyclable heterogeneous cobalt complex [J]. Journal of Molecular Catalysis A: Chemical, 2005, 232(1/2): 95-99

[3]

KoguchiS., KitazumeT.. Synthetic utilities of ionic liquid-supported NHPI complex [J]. Tetrahedron Lett, 2006, 47(16): 2797-2801

[4]

CoseriS., MendenhallG. D., IngoldK. U.. Mechanisms of reaction of aminoxyl (nitroxide), iminoxyl, and imdoxyl radicals with alkenes and evidence that in the presence of lead tetraacetate, N-Hydroxyphthalimide reacts with alkenes by both radical and nonradical mechanisms [J]. Journal of Organic Chemistry, 2005, 70(12): 4629-4636

[5]

IshiiY., SakaguchiS.. A new strategy for alkane oxidation with O2 using N-hydroxyphthalimide(NHPI) as a radical catalyst [J]. Catalysis Surveys from Japan, 1999, 3(1): 27-35

[6]

IWAHAMA T, HATTA G, SAKAGUCHI S, ISHII Y. Epoxidation of alkenes using alkyl hydroperoxides generated in situ by catalytic autoxidation of hydrocarbons with dioxygen [J]. Chemical Communications, 2000(2): 163–164.

[7]

JiangS.-c., WuY., LiJ., LiüZ.-p., LiuHui.. Synthesis of rare fragrance precursor used in tobacco [J]. Fragrance Flavor Cosmetic, 2003, 5(5): 5-6

[8]

AleuJ., BrennaE., FugantiC., SerraS.. Lipase-mediated synthesis of the enantiomeric forms of 4,5-epoxy-4,5-dihydro-α-ionone and 5, 6-epoxy-5, 6-dihydro-β-ionone: A new direct access to enantiopure (R)-and (S)-α-ionone[J]. Journal of the Chemical Society, Perkin Transactions. 1: Organic and Bio-Organic Chemistry, 1999, 999(3): 271-278

[9]

LiuJ., ColmenaresL. U., LiuR. S. M.. Fluorinated astaxanthins [J]. Tetrahedron Lett, 1997, 38(49): 8495-8498

[10]

LuoY.-m., LiuC.-h., TangR.-r., YangH.-wu.. Synthesis of 4-oxo-β-ionone by oxidation of sodium chlorate [J]. Journal of Central South University: Science and Technology, 2006, 37(3): 521-526

[11]

PENG Qian-rong, YANG Min, XIE Ru-gang, SONG Guang-fu, LIU Zhong-xiang, WANG Dong-shan, CAI Yuan-qing. A synthesis method of oxo-α-ionone, oxo-β-ionone and their ether and ester derivatives by one step. China: 1817842A [P]. 2006-08-16. (in Chinese)

[12]

ZhuoG.-l., ZhaoW.-j., JiangX.-zhen.. A novel catalyst system for the oxidation of toluene to benzoic acid [J]. Chinese Journal of Organic Chemistry, 2004, 24(8): 962-965

[13]

HiraiN., SawatariN., NakamuraN., SakaguchiS., IshiiY.. Oxidation of substituted toluenes with molecular oxygen in the presence of N, N′, N″-trihydroxyisocyanuric acid as a key catalyst [J]. Journal of Organic Chemistry, 2003, 68(17): 6587-6590

[14]

TangR.-r., LiuC.-h., LuoY.-m., GuoC.-cheng.. Studies on the catalytic oxidation of β-ionone to 4-oxo-β-ionone [J]. Journal of Applied Chemistry, 2006, 23(7): 718-723

[15]

SheldonR. A., ArendsI. W. C. E.. Organocatalytic oxidations mediated by nitroxyl radicals [J]. Advanced Synthesis and Catalysis, 2004, 346(9/10): 1051-1071

[16]

FanQ., LiY.-z., ChengP.-m., HuJ.-y., LiX.-jun.. Studies on allylic oxidation in cyclohexene [J]. Chemical Research and Application, 2001, 13(5): 557-559

[17]

IshiiY., SakaguchiS.. Recent progress in aerobic oxidation of hydrocarbons by N-hydroxyimides [J]. Catalysis Today, 2006, 117(1/3): 105-113

AI Summary AI Mindmap
PDF

155

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/