Synthesis of new sulfonic acid derivatives by the reaction of S-(1S,2R,3S,5R)-2-formyl-6,6-dimethylnorpinan-3-yl thioacetate with chlorine dioxide

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New polyfunctional compounds of the pinane series, 2-carboxy-3-thioacetate, 2-carboxy-3-sulfonyl chloride, and 2-carboxy-3-sulfonic acid that are promising intermediate products in organic synthesis, were synthesized for the first time by the reaction of S-(1S,2R,3S,5R)-(6,6-dimethyl-2-formylnorpinan-3-yl) thioacetate with chlorine dioxide. The major reaction pathway in nonpolar solvents involves oxidation of the aldehyde group to carboxy, whereas oxidation of the sulfur atom, followed by deacetylation, occurs in highly polar solvents. The effect of VO(acac)2 as catalyst on the reaction chemoselectivity in weakly polar diethyl ether was revealed.

作者简介

S. Subbotina

Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: lezina-om@yandex.ru
ORCID iD: 0009-0001-0512-3478
俄罗斯联邦, ul. Pervomayskaya, 48, Syktyvkar, 167000

O. Grebyonkina

Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: lezina-om@yandex.ru
ORCID iD: 0000-0002-1982-104X
俄罗斯联邦, ul. Pervomayskaya, 48, Syktyvkar, 167000

P. Gribkov

Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: lezina-om@yandex.ru
ORCID iD: 0000-0003-2923-4620
俄罗斯联邦, ul. Pervomayskaya, 48, Syktyvkar, 167000

D. Gerasimova

Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences

Email: lezina-om@yandex.ru
ORCID iD: 0000-0001-9770-196X
俄罗斯联邦, ul. Arbuzova, 8, Kazan, 420088

O. Lodochnikova

Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences

Email: lezina-om@yandex.ru
ORCID iD: 0000-0001-9614-5092
俄罗斯联邦, ul. Arbuzova, 8, Kazan, 420088

I. Gilfanov

Kazan National Research Technological University

Email: lezina-om@yandex.ru
ORCID iD: 0000-0003-4351-3378
俄罗斯联邦, ul. K. Marksa, 68, Kazan, 420015

L. Nikitina

Kazan State Medical University

Email: lezina-om@yandex.ru
ORCID iD: 0000-0003-2113-5732
俄罗斯联邦, ul. Butlerova, 49, Kazan, 420012

O. Lezina

Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: lezina-om@yandex.ru
ORCID iD: 0000-0002-6105-5641
俄罗斯联邦, ul. Pervomayskaya, 48, Syktyvkar, 167000

S. Rubtsova

Institute of Chemistry, Federal Research Center, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: lezina-om@yandex.ru
ORCID iD: 0000-0003-1224-8751
俄罗斯联邦, ul. Pervomayskaya, 48, Syktyvkar, 167000

参考

  1. Paduch R., Kandefer-Szerszen M., Trytek M., Fiedurek J. Arch. Immun. Ther. Exp. 2007, 55, 315–327. doi: 10.1007/s00005–007–0039–1
  2. Яровая О.И., Салахутдинов Н. Ф. Усп. хим. 2021, 90, 488–510. [Yarovaya O. I., Salakhutdinov N. F. Russ. Chem. Rev. 2021, 90, 488–510.] doi: 10.1070/RCR4969
  3. Соколова А.С., Баранова Д. В., Яровая О. И., Баев Д. С., Полежаева О. А., Зыбкина А. В., Щербаков Д. Н., Толстикова Т. Г., Салахутдинов Н. Ф. Изв. АН. Сер. Хим. 2019, 68, 1041–1046. [Sokolova A. S., Baranova D. V., Yarovaya O. I., Baev D. S., Polezhaeva O. A., Zybkina A. V., Shcherbakov D. N., Tolstikova T. G., Salakhutdinov N. F. Russ. Chem. Bull. 2019, 68, 1041–1046.] doi: 10.1007/s11172–019–2517–0
  4. Никитина Л.Е., Киселев С. В., Старцева В. А., Лодочникова О. А., Рахматуллина А. А., Федюнина И. В., Гильфанов И. Р., Изв. АН. Сер. Хим. 2019, 68, 1031–1035. [Nikitina L. E., Kiselev S. V., Startseva V. A., Lodochnikova O. A., Rakhmatullina A. A., Fedyunina I. V., Gilfanov I. R., Russ. Chem. Bull., 2019, 68, 1031–1035.] doi: 10.1007/s11172–019–2515–2
  5. Гребенкина О.Н., Лезина О. М., Изместьев Е. С., Судариков Д. В., Пестова С. В., Рубцова С. А., Кучин А. В. ЖОрХ. 2017, 53, 844–852. [Grebyonkina O. N., Lezina O. M., Izmest’ev E.S., Sudarikov D. V., Pestova S.V, Rubtsova S. A, Kutchin A. V. Russ. J. Org. Chem. 2017, 53, 860–868.] doi: 10.1134/S1070428017060082
  6. Lezina O.M., Subbotina S. N., Frolova L. L., Rubtsova S. A., Sudarikov D. V. Molecules. 2021, 26, 5245–5259. doi: 10.3390/molecules26175245
  7. Котегов Н.А., Белогурова Н. В., Зырянов В. А., Тупикина В. Г., Петров А. Ю. Пат. 2119332. (1995) РФ. Б.И. 1998, № 27.
  8. Гребенкина О.Н., Лезина О. М., Изместьев Е. С., Фролова Л. Л., Рубцова С. А., Кучин А. В. ЖОрХ. 2019, 55, 1510–1519. [Grebyonkina O. N., Lezina O. M., Izmest’ev E.S., Frolova L. L., Rubtsova S. A., Kutchin A. V. Russ. J. Org. Chem. 2019, 55, 1469–1475]. doi: 10.1134/S0514749219100045
  9. Лезина О.М., Гребенкина О. Н., Судариков Д. В., Крымская Ю. В., Рубцова С. А., Кучин А. В. ЖОрХ, 2015, 51, 1391–1398. [Lezina O. M., Grebyonkina O. N., Sudarikov D. V., Krymskaya Yu.V., Rubtsova S. A., Kutchin A. V. Russ. J. Org. Chem. 2015, 51, 1359–1367.] doi: 10.1134/S1070428015100012
  10. Nishiguchi A., Maeda K., S. Miki. Synthesis. 2006, 24, 4131–4134. doi: 10.1055/s-2006–950353
  11. Kim D.W., Ko Y. K., Kim S. H. Synthesis. 1992, 12, 1203–1204. doi: 10.1055/s-1992–26333
  12. Kværnø L., Werder M., Hauser H., Carreira E. M. Organic Lett. 2005, 7, 1145–1148. doi: 10.1021/ol0502127
  13. Humljana J., Gobec S. Tetrahedron Lett. 2005, 46, 4069–4072. doi: 10.1016/j.tetlet.2005.04.011
  14. Monnee M.C.F., Marijne M. F., Brouwer A. J., Liskamp R. M. Tetrahedron Lett. 2000, 41, 7991–7995. doi: 10.1016/s0040–403901387–3
  15. Martı́nez-Ramos F., Vargas-Dı́az M.E., Chacón-Garcı́a L., Tamariz J., Joseph-Nathan P., Zepeda L. G. Tetrahedron Asym. 2001. 12, 3095–3103. doi: 10.1016/S0957–416600545–6
  16. Якупов М.З., Ляпина Н. К., Шерешовец В. В., Имашев У. Б. Кинет. Катал. 2001, 42, 673–676. [Yakupov M. Z., Lyapina N. K., Shereshovets V. V., Imashev U. B. Kinet. Catal. 2001, 42, 609.] doi: 10.1023/A:1012307311387
  17. Krause L., Herbst-Irmer R., Sheldrick G. M., Stalke D. J. Appl. Crystallogr. 2015, 48, 3–10. doi: 10.1107/s1600576714022985
  18. Sheldrick G. M. Acta Crystallogr., Sect. A: Found. Adv. 2015, 71, 3–8. doi: 10.1107/S2053273314026370
  19. Sheldrick G. M. Acta Crystallogr., Sect. C: Struct. Chem. 2015, 71, 3–8. doi: 10.1107/S2053229614024218
  20. Dolomanov O.V., Bourhis L. J., Gildea R. J., Howard J. A.K., Puschmann H. J. J. Appl. Crystallogr. 2009, 42, 339–341. doi: 10.1107/S0021889808042726
  21. Spek A. L. Acta Crystallogr., Sect. D: Biol. Crystallogr. 2009, 65, 148.
  22. Macrae C.F., Sovago I., Cottrell S. J., Galek P. T.A., McCabe P., Pidcock E., Platings M., Shields G. P., Stevens J. S., Towler M., Wood P. A. J. Appl. Crystallogr. 2020, 53, 226–235. doi: 10.1107/S1600576719014092
  23. Петренко Н.Ф., Мокиенко А.В. Диоксид хлора: применение в технологиях водоподготовки. Одесса: Optimum. 2005, 371.
  24. Rowe Р.А., Jones М. М. Inorganic Syntheses. Ed. Th. Moeller. N.Y.–Toronto–London: McGraw-Hill Book Company, Inc. 1957, 5, 113–116. doi: 10.1002/9780470132364.ch30
  25. Изместьев Е.С., Петухов Д. В., Пестова С. В., Рубцова С. А. ЖОрХ. 2023, 59, 106–118. [Izmest’ev E.S., Petukhov D. V., Pestova S. V., Rubtsova S. A. Russ. J. Org. Chem. 2023, 59, 67–77.] doi: 10.31857/S0514749223010093

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