SOME time ago we have shown that the sulphonic acid obtained in the remarkable sulphonation of 2,6-di-tert.-butylpyridine (I) with sulphur trioxide in liquid sulphur dioxide at -10' according to Brown and Kanner -1 is not the b-derivative (III) as suggested by these investigators but the 34erivative
✦ LIBER ✦
Syntheses of 2,6-DI-t-Butylpyridine-3-and −4–sulphonic acids
✍ Scribed by H. C. van der Plas; H. J. den Hertog
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 571 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
Syntheses of 2,6‐di‐t‐butylpyridine‐3‐ and −4‐sulphonic acids proving the structure of these compounds are described. They were carried out in order to confirm that during the sulphonation of 2,6‐di‐t‐butylpyridine at low temperature the sulphonic acid group enters the 3‐position.
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