Synthesis of acetylene triols

Abdirazokov, Allanazar, Khaydarova, Zubayda E., Abdulloev, Shakhobidin Kh.

Товарлар кимёси ва халқ табобати · 2024-yil

Annotatsiya

The data of studies aimed at obtaining biologically active compounds of the acetylene series are presented. Methods have been developed for the production of simple monoesters of acetylene triols, which include: condensation under the conditions of the Favorsky reaction of 1-alkoxy-pentine-2-ols with acetone in liquid ammonia at a temperature of (-30–-35) °C in the presence of powdered caustic potassium. In this way, 6 new representatives of simple monoesters of acetylene triols were synthesized. It was found that the highest yield of the final product corresponds to an essential radical with methyl and ethyl groups. With an increase in the length of the alkyl radical, the yield of the final products decreases. To prove the composition and structure of the synthesized compounds, the reaction of splitting them into initial products- 1-alkoxy-pentine-2-ols and acetone when heated in the presence of K2CO3 (Favorsky reverse reaction), IR spectral data and elemental analysis were used. The test data of synthesized compounds are presented.

Maqola ma’lumotlari
MualliflarAbdirazokov, Allanazar, Khaydarova, Zubayda E., Abdulloev, Shakhobidin Kh.
JurnalТоварлар кимёси ва халқ табобати
NashriyotТабобат академияси
ISSN2181-2977
Nashr sanasi2024-12-19
Jild3
Son4
Betlar68-80
TilIngliz
Ilmiy sohaKimyo
DOI10.55475/jcgtm/vol3.iss4.2024.362
Indeksga qo‘shilgan2026-08-26

DOI: 10.55475/jcgtm/vol3.iss4.2024.362 · Maqolaning asl sahifasi

Kalit so‘zlar

алкоксиацетиленовый спирт, кетоны, рованные кратные связи, простые моноэфиры тритретичных ениновых триолов, реакция Фаворского, alkoxyacetylene alcohol, ketones, isolated multiple bonds, simple monoesters of tritretic enin triols, Favorsky reaction, alkoksiasetilen spirti, ketonlar, izolyatsiya qilingan karrali bog'lanishlar, tritretik enin triollarining oddiy monoefirlari, Favorskiy reaktsiyasi

Ilmiy soha

Kimyo

Iqtibos keltirish

APAAbdirazokov, Allanazar, Khaydarova, Zubayda E., & Abdulloev, Shakhobidin Kh. (2024). SYNTHESIS OF ACETYLENE TRIOLS. Товарлар кимёси ва халқ табобати, 3(4), 68-80. https://doi.org/10.55475/jcgtm/vol3.iss4.2024.362
GOST (OAK)Abdirazokov, Allanazar, Khaydarova, Zubayda E., Abdulloev, Shakhobidin Kh. SYNTHESIS OF ACETYLENE TRIOLS // Товарлар кимёси ва халқ табобати. – 2024. – T. 3, № 4. – P. 68-80. – DOI: 10.55475/jcgtm/vol3.iss4.2024.362.
MLAAbdirazokov, Allanazar, Khaydarova, Zubayda E., and Abdulloev, Shakhobidin Kh. “SYNTHESIS OF ACETYLENE TRIOLS.” Товарлар кимёси ва халқ табобати, 3(4), 68-80, 2024. https://doi.org/10.55475/jcgtm/vol3.iss4.2024.362
ChicagoAbdirazokov, Allanazar, Khaydarova, Zubayda E., and Abdulloev, Shakhobidin Kh. “SYNTHESIS OF ACETYLENE TRIOLS.” Товарлар кимёси ва халқ табобати, 3(4), 68-80 (2024). https://doi.org/10.55475/jcgtm/vol3.iss4.2024.362
HarvardAbdirazokov, Allanazar, Khaydarova, Zubayda E., and Abdulloev, Shakhobidin Kh (2024) ‘SYNTHESIS OF ACETYLENE TRIOLS’, Товарлар кимёси ва халқ табобати, 3(4), 68-80. https://doi.org/10.55475/jcgtm/vol3.iss4.2024.362
BibTeX
@article{abdirazokovallanazar2024,
  title = {SYNTHESIS OF ACETYLENE TRIOLS},
  author = {Abdirazokov, Allanazar and Khaydarova, Zubayda E. and Abdulloev, Shakhobidin Kh.},
  journal = {Товарлар кимёси ва халқ табобати},
  year = {2024},
  volume = {3},
  number = {4},
  pages = {68-80},
  doi = {10.55475/jcgtm/vol3.iss4.2024.362},
  url = {https://doi.org/10.55475/jcgtm/vol3.iss4.2024.362}
}

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