## 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‐positio
Synthesis of the isomeric sulphonic acids of 2,6-di-tert.-butylpyridine
✍ Scribed by H.C. van der Plas; H.J. den Hertog
- Publisher
- Elsevier Science
- Year
- 1960
- Tongue
- French
- Weight
- 214 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
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 (II) 2. Recently our conclusion was affirmed by the results of an examination of the nuclear magnet resonance spectrum of the sulphonic acid by Muller and Wallace 3.
In this letter a definitive proof is given by syntheses of both II and III from 4-ethoxypyridine (IV) and 4-thiomethylpyridine (V) respectively. ic
📜 SIMILAR VOLUMES
## Abstract Convenient procedures for the synthesis of 2,6‐di‐tert‐butyl‐4‐methylphenol (ionol) mono‐, di‐, and triphosphorus derivatives, starting from the readily accessible 3,5‐di‐tert‐butyl‐4‐hydroxybenzaldehyde, are proposed, and some properties of the obtained compounds are presented. © 2008
## Abstract 2, 6‐Di‐__tert__‐butyl‐p‐cresol‐^14^C~6~ was synthesised by reacoting __p__‐cresol‐^14^C~6~ with isobutylene using concetentrated sulfurica acid as catalyst. Purification of the Labelled butylated __p__‐cresol involved very careful recrystalliation of this product from absolute alcohol