## Abstract The synthesis of hexabenz‐1,12;2,3;4,5;6,7;8,9;10,11‐coronene, using two different reaction schemes is described. The cyclodehydrogenation of hexaphenylbenzene, and the reaction of dibenz‐1,9;2,3‐anthrone with Zn/ZnCl~2~ lead to identical products, the chemical and crystallographic prop
✦ LIBER ✦
Odeur et constitution XI. Etude de la transestérification-déshydratation de la lactone de l'acide tétraméthyl-1,1,6,10-hydroxy-6-décalyl-5-acétique
✍ Scribed by M. Stoll; M. Hinder
- Publisher
- John Wiley and Sons
- Year
- 1954
- Tongue
- German
- Weight
- 498 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The transesterification‐dehydration of lactone I (of 1, 1, 6, 10‐tetramethyl‐6‐hydroxy‐decalyl‐5‐acetic acid) yields besides small quantities of isolactone II the ester of the corresponding non saturated acid III. Prolonged heating in the presence of more concentrated sulfuric acid isomerizes this acid into acid IV. If the concentration of the latter reaches 45%, saponification of the reaction products yields no more the acids III m. p. 118° or IV m. p. 102° but an eutectic acid m. p. 84°. The corresponding infrared spectra are discussed.
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Synthèses dans la série des dérivés poly
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A. Halleux; R. H. Martin; G. S. D. King
📂
Article
📅
1958
🏛
John Wiley and Sons
🌐
German
⚖ 448 KB