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1-aralkylated tetrahydro-2-benzazepines. Part II: Synthesis from 3-(3,4-dimethoxyphenyl)-propylamine

✍ Scribed by Daniel Berney; Theodor Jauner


Publisher
John Wiley and Sons
Year
1976
Tongue
German
Weight
280 KB
Volume
59
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

3‐(3,4‐Dimethoxyphenyl)‐propylamine was N‐acylated with aralkanecarboxylic acid chlorides. The resulting amides were subjected to Bischler‐Napieralski ring closure to give the corresponding 1‐aralkyl‐dihydro‐2‐benzazepines. These were reduced to the title compounds.


📜 SIMILAR VOLUMES


1-Aralkylated Tetrahydro-2-benzazepines.
✍ Daniel Berney; Karlheinz Schuh 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 German ⚖ 626 KB

## Abstract 1‐Benzyl‐tetrahydro‐2‐benzazepin‐3‐ones **4** were prepared by submitting the corresponding 1‐benzyl‐β‐tetralones **3** to the __Schmidt__ reaction. On the other hand, the rearrangement of the tetralones **3** by the __Beckmann__ procedure gave 1‐benzyl‐tetrahydro‐3‐benzazepin‐2‐ones **

A New Synthesis of Phenolic 1-Hydroxy-1-
✍ Motoki Ikeuchi; Miyuki Ikeuchi; Kumiko Inoue; Syuhei Yamamoto; Aiko Yamauchi; Ma 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

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