## Abstract The reaction of 4,5‐dihydro‐2‐morpholino‐ (and ‐2‐pyrrolidino)‐3‐furancarbonitriles 1a, c, d and 2a, c, d with dichlorocarbene gave 4‐(2,4‐pentadienoyl)morpholines 3a, c, d and 1‐(2,4‐pentadienoyl)pyrrolidines 4a, c, d. Similarly, the reaction of 4,5‐dihydro‐5‐methyl‐2‐morpholino‐ (and
Studies on Heterocyclic Enaminonitriles, XIII. Reactions of EthylN-2-(3-Cyano-4,5-dihydro-2-furyl)carbamates with Sodium Iodide
✍ Scribed by Maruoka, Hiroshi ;Yamagata, Kenji ;Yamazaki, Motoyoshi
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 338 KB
- Volume
- 1993
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
The reaction of ethyl N‐2‐(3‐cyano‐4,5‐dihydro‐2‐furyl)carbamate (1), 1‐cyano‐N‐(ethoxycarbonyl)cyclopropanecarboxamide (2), and ethyl 3‐cyano‐2‐oxo‐1‐pyrrolidinecarboxylate (3) with sodium iodide gave 3‐ethyl‐2‐oxo‐3‐pyrrolidinecarbonitrile (5). Similarly, the reaction of ethyl N‐2‐[3‐cyano‐4,5‐dihydro‐4‐(or ‐5‐)phenyl‐2‐furyl]carbamate (7 or 8) and trans‐1‐cyano‐N‐(ethoxycarbonyl)‐2‐phenylcyclopropane‐carboxamide (9) afforded 3‐ethyl‐2‐oxo‐5‐phenyl‐3‐pyrrolidinecarbonitrile (10).
📜 SIMILAR VOLUMES
## Abstract The reactions of 2‐benzamido‐4,5‐dihydro‐3‐thiophene‐ and ‐3‐furancarbonitriles (1 and 2) with ethyl or methyl cyanoacetate and malononitrile (2 equiv.) in the presence of sodium hydride (1 equiv.) in dimethyl sulfoxide at 140°C gave ethyl or methyl cyano[3‐cyano‐4,5‐dihydro‐2(3__H__)‐t