Ammonium salts as economical and eco-friendly N-sources applied to green, simple and scale-up synthesis of trialkyl amines in water

Publish Year: 1399
نوع سند: مقاله ژورنالی
زبان: English
View: 412

This Paper With 9 Page And PDF Format Ready To Download

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

JR_ICC-8-2_003

تاریخ نمایه سازی: 12 مرداد 1399

Abstract:

We have introduced a selective synthesis of tertiary amines using alkyl halide and ammonium salts as the amine sources in water. This green process has outstanding superiorities, such as being eco-friendly, possessing ammonium salts, and using water as a green solvent in the absence of organic ligands or catalysts. It is worth mentioning that the presence of t-Butyl alcohol and potassium hydroxide leads to synthesize tertiary amines, while under other conditions we witnessed the formation of byproducts. Other factors affecting the synthesis of various tertiary amines are temperature ranges. Note that various tertiary amines and the process of scale-up were synthesized in moderate to high yields.

Authors

Elahe Ghiasbeigi

Departmant of Chemistry, Ilam University, P.O. BOX ۶۹۳۱۵-۵۱۶, Ilam, Iran

Mohammad Soleiman-Beigi

Departmant of Chemistry, Ilam University. PO.Box ۶۹۳۱۵-۵۱۶, Ilam, Iran

مراجع و منابع این Paper:

لیست زیر مراجع و منابع استفاده شده در این Paper 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 Paper لینک شده اند :
  • H. Ohta, Y. Yuyama, Y. Uozumi,  Y.M.A. Yamada, Org. Lett., ...
  • (a) N. Rasouli, M. Movahedi, E. Aghabeikzadeh Naeini, Iran. Chem. ...
  • (a) M. Soleiman-Beigi, F. Mohammadi, M. Alikarami. Org. Chem. Res., ...
  • (a) J.N. Adamson, H. Jeddi, S.J. Malcolmson. J. Am. Chem. ...
  • D. Castagnolo, S. Schenone, M. Botta. Chem. Rev., 2011, 111, ...
  • M. Sun, C. Hong, C. Pan,  J. Am. Chem. Soc., ...
  • C. Prasad, A. Ragan.  J. Liq. Chromatogr., 1994, 17, 2383-2394. ...
  • Y. Kumatabara, M. Okada, S. Shirakawa, ACS Sustain. Chem. Eng., ...
  • L. Wang, Y. Eguchi, E.X.Y. Chen, Ind. Eng. Chem. Res., ...
  • B.J. Simmons, M. Hoffmann, J. Hwang, M.K. Jackl, N.K. Garg, ...
  • H. Huang, J.Y.J. Kang, J. Org. Chem., 2017, 82, 6604-6614. ...
  • T. Lim, S. Byun, and B.M. Kim, Asian J. Org. ...
  • M.A. Marsini, F.G. Buono, J.C. Lorenz, B.S. Yang, J.T. Reeves, ...
  • K. Fujita, Z. Li, R. Yamaguchi, Tetrahedron Lett., 2003, 44, ...
  • X. Cui, X. Dai, Y. Deng, F. Shi, Chem. - ...
  • K.I. Fujita, R. Yamaguchi, Synlett., 2005, 2005, 560-571 ...
  • L. He, Y. Qian, R.S. Ding, Y.M. Liu, H.Y. He, ...
  • (a) Q. Lu, P. Chen, M. Addy, R. Zhang, X. ...
  • Y. Chen, Y. Wu, C. Liu, L. Guo, J. Nie, ...
  • R.R. Karri , J.N. Sahu, V. Chimmiri, J. Mol. Liq., ...
  • M. Soleiman-Beigi, F. Mohammadi, Monatshefte fur Chemie., 2017, 148, 2123-2128. ...
  • Y. Ren, S. Jin, J. Adv. Oxid. Technol.,  2017, 20. ...
  • M.A. Zolfigol, M. Safaiee, F. Afsharnadery, N. Bahrami-Nejad, S. Baghery, ...
  • T.S. Ahooie, N. Azizi, I. Yavari, and M.M. Hashemi, J. ...
  • W. Zhang, X. Dong, W. Zhao, Org. Lett., 2011, 13, ...
  • S. Liu, R. Chen, G. Deng, Chem. Lett., 2011, 40, ...
  • E.S. Berman , S.L. Fortson, K.D. Checchi, L. Wu, J.S. ...
  • Australia New Zealand Food Standards Code  Standard 1.2.4 - Labelling ...
  • (a) T. Shamim, V. Kumar, S. Paul, Synth. Commun., 2014, ...
  • (a) P.J. DeChristopher, J.P. Adamek, G.D. Lyon, J.J. Galante, H.E. ...
  • A. Gioiello, E. Rosatelli, M. Teofrasti, P. Filipponi, and R. ...
  • (a) N.M. Brouwer, P.M.J. Terpstran, Tenside surfactants detergents., 1995, 32, 225-228; ...
  • نمایش کامل مراجع