STUDY OF THE REACTION OF м-FERROCENYL BENZOIC ACID WITH METHYLOLDITHIOUREA

I Askarov; M Khojimatov; F Abdugapparov

Chemistry

No. 5 (2020): Scientific journal of the Fergana State University

STUDY OF THE REACTION OF м-FERROCENYL BENZOIC ACID WITH METHYLOLDITHIOUREA

I.Askarov^▸^▾
M.Khojimatov^▸^▾
F.Abdugapparov^▸^▾

PDF (Uzbek)

Submitted: July 3, 2023
Published: 2023-07-05

Abstract

This article presents the method of synthesis of m-ferrocenyl benzoic acid with methyloldithiourea and the results of IR spectroscopy and mass spectrometry analysis proving the structure of the new substance obtained.

References

Снегур Л.В., Сименел А.А., Родионов А.Н., Боев В.И. Ферроцен-модификация органических соединений для медицинского применения// Известия Академии Наук. Серия химическая. 2014.№ 1
Suh John T., Colgate Palmolive Co, Novel processes for preparing ferrocene-cyclic ethers, US, Pat. № 3408376 A, 1968.3. Nesmeyanov A. N., Bogomolova L. G., Andrianova I. G., Vil’chevskaya V. D., Kochetkova N. S. “A new preparation (ferroseron) for the treatment of iron-de˶ciency anemia”, Pharmaceutical Chemistry Journal, 1972, vol. 6, no. 4.
Carlos Anjo a, J. Albertino Figueiredo a,M. Isabel Ismael a, Ivвnia Cabrita b, Ana C. Fernandes b. Synthesis of ferrocene derivatives functionalized with a-methylene-g-butyrolactone rings. Journal of Organometallic Chemistry 760 (2014) 19-235.
Pejovic A.,Damljanovic I.S., Stevanovic D., Vukicevic M.D, Novakovic S.B, Bogdanovic G.A, Radulovic N.S., Vukicevic R.D. Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives. Polyhedron 2012; 31(1):789-795. IF 2.057 44.
Ferrocene-containing carbohydrate surfactant: thermotropic and lyotropic phase behavior / B. Donnio [et al.] // Organometallics. – 2000. – Vol. 19, N 16.
Frank Strehler, Marcus Korb, Tobias Rьffer, Alexander Hildebrandt, Heinrich Lang. Synthesis and isomerization behavior of cyano-vinyl ferrocenes. Journal of Organometallic Chemistry 820 (2016) 89-978. Аскаров И.Р. Производные ферроцена. ─ Фергана, 1999.
Асқаров И.Р., Хожиматов М.М., Исақов Х., Қирғизов. Метилолмочевинанинг айрим ҳосилалари синтези//Илмий хабарнома. Андижон. -2014.-№4.
Asqarov I.R., Xojimatov M.M. Ferrocene and reaction metilolurea // Eastern European Scientific Journal. Германия. -2017.-№2.

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[1] Снегур Л.В., Сименел А.А., Родионов А.Н., Боев В.И. Ферроцен-модификация органических соединений для медицинского применения// Известия Академии Наук. Серия химическая. 2014.№ 1

[2] Suh John T., Colgate Palmolive Co, Novel processes for preparing ferrocene-cyclic ethers, US, Pat. № 3408376 A, 1968.3. Nesmeyanov A. N., Bogomolova L. G., Andrianova I. G., Vil’chevskaya V. D., Kochetkova N. S. “A new preparation (ferroseron) for the treatment of iron-de˶ciency anemia”, Pharmaceutical Chemistry Journal, 1972, vol. 6, no. 4.

[3] Carlos Anjo a, J. Albertino Figueiredo a,M. Isabel Ismael a, Ivвnia Cabrita b, Ana C. Fernandes b. Synthesis of ferrocene derivatives functionalized with a-methylene-g-butyrolactone rings. Journal of Organometallic Chemistry 760 (2014) 19-235.

[4] Pejovic A.,Damljanovic I.S., Stevanovic D., Vukicevic M.D, Novakovic S.B, Bogdanovic G.A, Radulovic N.S., Vukicevic R.D. Antimicrobial ferrocene containing quinolinones: Synthesis, spectral, electrochemical and structural characterization of 2-ferrocenyl-2, 3-dihydroquinolin-4(1H)-one and its 6-chloro and 6-bromo derivatives. Polyhedron 2012; 31(1):789-795. IF 2.057 44.

[5] Ferrocene-containing carbohydrate surfactant: thermotropic and lyotropic phase behavior / B. Donnio [et al.] // Organometallics. – 2000. – Vol. 19, N 16.

[6] Frank Strehler, Marcus Korb, Tobias Rьffer, Alexander Hildebrandt, Heinrich Lang. Synthesis and isomerization behavior of cyano-vinyl ferrocenes. Journal of Organometallic Chemistry 820 (2016) 89-978. Аскаров И.Р. Производные ферроцена. ─ Фергана, 1999.

[7] Асқаров И.Р., Хожиматов М.М., Исақов Х., Қирғизов. Метилолмочевинанинг айрим ҳосилалари синтези//Илмий хабарнома. Андижон. -2014.-№4.

[8] Asqarov I.R., Xojimatov M.M. Ferrocene and reaction metilolurea // Eastern European Scientific Journal. Германия. -2017.-№2.