Reaction of N-tert-butyl-2-haloaldimines with thiolcarboxylic acids
- Авторы: Khairullin R.1, Gazizov M.1, Kirillina Y.1, Gazizova K.1, Khayarov K.1
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Учреждения:
- Kazan Research Technological University
- Выпуск: Том 87, № 11 (2017)
- Страницы: 2736-2738
- Раздел: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/221653
- DOI: https://doi.org/10.1134/S1070363217110342
- ID: 221653
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Аннотация
The reactions of N-tert-butyl-2-chloroaldimine with thiolcarboxylic acids occurs along two pathways: nucleophilic substitution of chlorine in the primary iminium salt by acylmercapto group and reduction of the C–Cl bond in the iminium cation. The reactions of thiolcarboxylic acids reaction with 2-bromoaldimine take exclusively the second pathway, specifically reduction of the C–Br bond in the cation of the primary iminium salt. Acylmercapro-substituted iminium salts and aldehydes and their acetals are synthesized.
Об авторах
R. Khairullin
Kazan Research Technological University
Email: mukattisg@mail.ru
Россия, ul. K. Marksa 68, Kazan, Tatarstan, 420015
M. Gazizov
Kazan Research Technological University
Автор, ответственный за переписку.
Email: mukattisg@mail.ru
Россия, ul. K. Marksa 68, Kazan, Tatarstan, 420015
Yu. Kirillina
Kazan Research Technological University
Email: mukattisg@mail.ru
Россия, ul. K. Marksa 68, Kazan, Tatarstan, 420015
K. Gazizova
Kazan Research Technological University
Email: mukattisg@mail.ru
Россия, ul. K. Marksa 68, Kazan, Tatarstan, 420015
Kh. Khayarov
Kazan Research Technological University
Email: mukattisg@mail.ru
Россия, ul. K. Marksa 68, Kazan, Tatarstan, 420015