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Highly Efficient and Facile Green Approach for One-Pot Fischer Indole Synthesis
Highly Efficient and Facile Green Approach for One-Pot Fischer Indole Synthesis
Journal of the Korean Chemical Society. 2010. Aug, 54(4): 411-413
Copyright © 2010, The Korean Chemical Society
  • Received : December 14, 2009
  • Accepted : April 08, 2010
  • Published : August 20, 2010
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About the Authors
Atul Chaskar
Dipartimento Di Chimica,Materiali Ed Ingegneria Chimica “Giulio Natta” Politecnico Di Milano, Italy
achaskar@rediffmail.com
Hrushikesh Deokar
Department of chemistry, Post graduate and Research Centre, C. K. Thakur College, Navi Mumbai, Maharashtra, 410206, India
Vikas Padalkar
Department of chemistry, Post graduate and Research Centre, C. K. Thakur College, Navi Mumbai, Maharashtra, 410206, India
Kiran Phatangare
Department of chemistry, Post graduate and Research Centre, C. K. Thakur College, Navi Mumbai, Maharashtra, 410206, India
S. K. Patil
Department of chemistry, Post graduate and Research Centre, C. K. Thakur College, Navi Mumbai, Maharashtra, 410206, India

Abstract
A simple, efficient and an environmental friendly method have been developed for the synthesis of substituted indole from aryl hydrazines and aldehydes/ ketones with HPA-phosphomolybdic acid as a heterogeneous catalyst. The catalyst is nontoxic and recyclable.
Keywords
INTRODUCTION
Indole and its derivatives are common heterocyclic compounds in nature which have attracted considerable interest in recent years due to their therapeutic and pharmacological activities. 1 - 3 Indole derivatives are used as neuroprotective agents affecting oxidative stress, 4 glucokinase activators, 5 , 6 neurotransmitter serotonin 7 (5-hydroxytriptamine 5-HT) involved in various physiological function such as appetite, sleep, body temperature and sexual behavior.8 Different indole derivatives like tryptans are used as antimigrain, antiinflammatory drugs, and dyestuffs. 8 , 9
Indoles can be prepared by numerous methods. However, all these methods have their own limitations and a number of drawbacks such as use of toxic solvents, expensive reagents, and amount of waste solvents. 10 - 13 Amongst the various approaches for the synthesis of indole, Fischer indole synthesis has mentioned its prominent role but reagent for Fischer indole synthesis such as conc. sulphuric acid, cuprous chloride, zinc chloride, borontrifluoide o-polyphpsporic acid, p-toluenesulphonic acid are hazardous to environment, difficult to handle and also required in very large amount. 14 With the increasing interest in human health and environmental protection, more attention is being paid to “green chemistry.” Therefore, it is necessary to develop an efficient, mild and practical method for the synthesis of indole.
In recent decades use of heteropoly acids (HPAs) as catalyst has become important in industries related with fine chemicals. 15 HPAs are more active catalyst than conventional inorganic and organic acids used for various reactions in solution. 16 Solid HPAs have gained importance due to easy work-up procedures, minimization of waste product generation. They are non-corrosive and environmentally benign, as they can be reused and recycled. 17 Thus keeping this in mind and as a part of our ongoing project to explore the catalytic activities of heteropoly acid in organic transformation, 18 here we have attempted the convenient and practical synthesis of substituted indole from commercially available aryl hydrazines, aldehydes/ketones and phosphomolybdic acid as heterogeneous catalyst ( 1 ).
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RESULTS AND DISCUSSION
The reaction of phenyl hydrazine hydrochloride with acetophenone was selected as model reaction to test the activity of different solid acid catalyst like zeolites-HY, Montmorillonite K10, Indion-90, Amberlite-120, Silica, Amberlyst-15, Phosphomolybdic acid at 60 ℃ in chloroform for 4 hrs.
The results mentioned in 1 demonstrate the efficient use of phosphomolybdic acid for Fischer indole synthesis. Keeping all these results in view, we generalized the protocol by treating various aldehydes and ketones with aryl hydrazine hydrochloride in presence of phosphomolybdic acid. Fischer indole synthesis of all the substrate was observed with 70 - 90% yield ( 2 ). Electron withdrawing group on aryl hydrazine lower the rate of reaction.
In eco-friendly process, the recovery of catalyst is the key step. In this protocol we used heteropoly acid as recyclable catalyst. After the completion of reaction, the heteropoly acid was recovered and used further for two more processes ( . 1 ).
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Recyclability of the catalyst
Effects of Catalysts on Fischer indole synthesis.a
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aPhenyl hydrazine hydrochloride (0.01 mol), acetophenone (0.01 mol), catalyst (0.002 mol), solvent (chloroform), Temp.: 60 ℃, Time: 4 hrs. bIsolated Yield (%).
Synthesis of substituted indoles.a
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aReaction conditions: Aryl hydrazine (0.01 mol), Aldehydes/Ketones (0.01 mol), Phosphomolybdic acid (0.002 mol), solvent: chloroform (5 mL). bIsolated Yield (%).
CONCLUSIONS
In conclusion, heteropolyacid phosphomolybdic acid has been proved useful, efficient and recyclable catalyst for Fischer indole synthesis. The catalytic activities of the heteropoly acid are much higher than those of conventional acid catalysts. It gives high yield in short reaction time.
EXPERIMENTAL SECTION
- General
All commercial reagents are used as received without purification and all solvents were of reagent grade. The reaction was monitored by TLC using 0.25 mm E-Merck silica gel 60 F 254 precoated plates, which were visualized with UV light. Melting points were observed using open capillaries. The IR spectra were recorded on a Perkin-Elmer 257 spectrometer using KBr discs. 1 H NMR spectra were recorded on VXR-300 MHz instrument using TMS as an internal standard.
- General Experimental Procedure
Acetophenone (0.01 mol) was mixed with phosphomolybdic acid (0.002 mol) in chloroform (5 mL) solvent at room temperature, to that phenyl hydrazine (0.01 mol) was added slowly at room temperature, then the reaction mixture was heated to 60 ℃ for 4 hrs. Completion of reaction was monitored by TLC; catalyst was separated from reaction mixture by filtration. The product obtained was purified by column chromatography.
- Representative spectral data for product
3-(1H-Indol-3-yl) propan-1-ol. IR (Neat): 3544, 3412, 2935, 2458, 1340, 1230, 1050, 743 cm -1 ; 1 H-NMR (CDCl 3 ) δ 8.05 (br s, 1H), 7.59 (d, 1H, J = 7.8 Hz), 7.26 (d, 1H, J = 7.8 Hz), 7.19 (t, 1H, J = 7.5 Hz), 7.08 (t, 1H, J = 7.5 Hz), 6.8 (s, 1H), 3.65 (t, 2H, J = 6.4), 2.9 (t, 2H, J = 7.5), 2.02 (m, 2H), 3.46 (br s, 1H) ppm; MS (EI, 70 eV) m/z 175 (M + ), 130 (100), 77 (15); Anal Calcd for C 11 H 13 NO: Calcd: C, 75.43; H, 7.43; N, 8.00; Found: C, 75.40; H, 7.45; N, 8.03.
Acknowledgements
Authors are grateful to University Grant Commission, New Delhi for financial support. Thanks to Dr. S. T. Gadade, Principal, C. K. Thakur College for providing laboratory and other facilities.
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