o-Bromoacetophenone reacts with the sodium salt of ethyl cyanoacetate to afford a-cyano-P-phenyl-A".Pbutenolide. This butenolide undergoes azo coupling with diazotized aromatic amines (ArNHJ to afford the hydrazo derivatives. These hydrazo derivatives (Ar= Ph, were transformed into the corresponding
✦ LIBER ✦
Some reactions of ω-chloroacetophenone and ω-chloro-p-methylacetophenone with phenylhydrazine and its substituted derivatives
✍ Scribed by A. P. J. Hoogeveen
- Book ID
- 104585196
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 491 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0165-0513
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