## 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 **
1-Aralkylated Tetrahydro-2-benzazepines. Part I: Synthesis from methoxylated phenylpropionamides
✍ Scribed by Daniel Berney; Karlheinz Schuh
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- German
- Weight
- 557 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
Phenylpropionamides acylated in the ortho position with aralkanecarboxylic acids were cyclised to give, after reduction, 1‐aralkyl‐tetrahydro‐2‐benzazepines.
📜 SIMILAR VOLUMES
## 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.
## Abstract Compound **2** was rearranged on treatment with 2N NaOH to the 2‐benzazepine‐3‐propanoicSee footnote (5) of the preceding paper. acid **3**. Some aspects of the chemistry of this acid were studied.
## Abstract For Abstract see ChemInform Abstract in Full Text.