Reusable Silica supported Perchloric acid and potassium bisulphate as green catalysts for thiocyanation of aromatic compounds under solvent free conditions

سال انتشار: 1395
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 276

فایل این مقاله در 12 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_ICC-5-3_014

تاریخ نمایه سازی: 2 مهر 1398

چکیده مقاله:

Reusable silica supported perchloric acid and potassium bisulphate have been prepared and explored as green catalysts for thiocyanation of aromatic compounds under conventional and solvent free microwave assisted conditions. The microwave assisted protocol exhibited remarkable rate accelerations and offered selective thiocyanation of aromatic and hetero aromatic compounds in good yields. Reaction times observed in conventional methods range of 2.0 to 6.0 hours, which reduced to only few minutes (1 to 3 min) in microwave assisted reactions. The developed protocols are also promising and comparable with the existing procedures. Prepared catalysts could be easily recycled for five time with a reproducible efficiency.

کلیدواژه ها:

Silica supported Potassium bisulfate ، silica supported HClO4 ، ammonium thiocyanate ، selective thiocyanation ، solvent free microwave assisted reactions ، rate accelerations

نویسندگان

Chinna Rajanna Kamatala

Department of Chemistry, Osmania University, Hyderabad (T.S)-۵۰۰۰۰۷ India

Hemanth Sriram Y.

Department of Chemistry Osmania University Hyederabad -(T.S) ۵۰۰۰۰۷ India

Satish Kumar Mukka

Department of Chemistry Osmania University Hyderabad-(T.S) India

Venkateswarlu Marri

Department of Chemistry Osmania Univerity Hyderabad-(T.S) India

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :
  • S. Rezayati, F. S. Farahani, Z.  Hossaini, R. Hajinasiri, S.  ...
  • K. Wilson, J.H. Clark, Pure Appl. Chem, 2000, 72, 1313-1319. ...
  • S. Sajjadifar, S. Karimian, H. Noorizadeh, H. Veisi, Journal of ...
  • L.Wu, C. Yang, C. Zhang, L. Yang, Lett. Org. Chem, ...
  • S. Rostamizadeh, N. Shadjou, A.M. Amani, S. Balalaie, Chinese Chem. ...
  • G.W. Breton, J. Org. Chem, 1997, 62, 8952- 8954. ...
  • C. Ramesh, J. Banerjee, R. Pal, B. Das, Adv. Synth. ...
  • M. Kaur, S. Sharma, P.M.S. Bedi, Chinese J. Catal, 2015, ...
  • A.T. Khan, T. Parvin, L.H. Choudhury, Synthesis, 2006, 2497-2502. ...
  • A.T. Khan, L.H. Choudhury, S. Ghosh. J. Mol. Cat. A: ...
  • V.T. Kamble, V.S. Jamode, N.S. Joshi, A.V. Biradar, R.Y. Deshmukh, ...
  • M.A. Bigdeli, M.M. Heravi, G.H. Mahdavinia, J. Mol. Cat. A: ...
  • M. Narasimhulu, T. Srikanth Reddy, K. Chinni Mahesh, P. Prabhakar, ...
  • B. Das, K. Damodar, N. Chowdhury, R. Aravind Kumar, J. ...
  • L.Q. Wu, Y.F. Wu, C.G. Yang, L.M. Yang, L.J. Yang, ...
  • G. Agnihotri, A.K. Misra, Tetrahedron Lett, 2006, 47, 3653. ...
  • S. Rudrawar, R.C. Besra, A.K. Chakraborti, Synthesis, 2006, 2767. ...
  • A. Agarwal, S. Rani, Y.D. Vankar, J. Org. Chem, 2004, ...
  • H.R. Shaterian, F. Shahrekipoor, M. Ghashang, J. Mol. Catal. A: ...
  • S. Pathak, K. Debnath, A. Pramanik, Beilstein J. Org. Chem., ...
  • G. Mukut, J.H. van Tonder, B.C.B. Benzuidenhoudt, Iran. J. Chem. ...
  • (a). J.L. Wood, Organic Reactions, New York: Wiley, 1967, 3, ...
  • R.G. Guy, In: S. Patai (Ed.), The Chemistry of Cyanates ...
  • J.S. Yadav, B.V.S. Reddy, S. Shubashree, K. Sadashiv, Tetrahedron Lett, ...
  • (a) R. Riemschneider, J. Am  Chem Soc, 1956, 78, 844; ...
  • Z.H. Zhang, L.S. Liebeskind, Org. Lett, 2006, 8, 4331-4333. ...
  • (a) T. Billard, B.R. Langlois, M. Medebielle, Tetrahedron Lett., 2001, ...
  • Y.T. Lee, S.Y. Choi, Y.K. Chung, Tetrahedron Lett, 2007, 48, ...
  • D.L. Mackinnon, P.A. Farrel, Environ. Toxicol. Chem, 1992, 11, 1541–1548. ...
  • G.M. Rajendra, L. Jinfang, C. Andreas, F.T. Cathy, H. Min. ...
  • (a). Wu. Guaili, Liu. Qiang, Shen. Yinglin, Wu. Wentao, Wu. ...
  • (a). B. Akhlaghinia, A.R. Pourali, M. Rahmani, Syn. Comm, 2012, ...
  • (a). X.Q. Pan, M.Y. Lei, J.P. Zou, W. Zhang, Tetrahedron ...
  • (a) N. Iranpoor, H. Firouzabadi, R. Azadi, Tetrahedron Lett, 2006, ...
  • (a). S. Jana, Shouvik Chattopadhyay, Inorganic Chem. Comm, 2013, 35, ...
  • (a) V. Sudhakar Chary, G. Krishnaiah, M. Satish Kumar, K.C. ...
  • I.P. Beletskaya, A.S. Sigeev, A.S. Peregudov, P. Petrovskii, Mendeleev Commun., ...
  • (a) E.R. Nezhad, S. Karimian, S. Sajjadifar, Journal of Sciences, ...
  • Z.N. Siddiqui., Arabian J. Chem., 2015,( In Press), ...
  • doi.org/10.1016/j.arabjc.2015.06.013 ...
  • (a). F.C. Küpper, M.C. Feiters, B. Olofsson, T. Kaiho, S. ...
  • (a) P. Anastas, J. Warner, In Green Chemistry: Theory and ...
  • P. Lidström, J. Tierney, B. Wathey, J. Westman, Tetrahedron, 2001, ...
  • (a). R.S. Varma, Green Chem, 1999, 1, 43–55; (b) P. ...
  • C. Oliver Kappe, Angew. Chem. Int. Ed, 2004, 43, 6250–6284. ...
  • C.R. Strauss, R.W. Trainor, Aust. J. Chem, 1995, 48, 1665–1692. ...
  • نمایش کامل مراجع