Synthesis of 3-Phenyl-, 3,4-Diphenyl-, and 3-(β-Naphthyl)-1,2,5-thiadiazole
✍ Scribed by Dr. V. Bertini; Prof. Dr. P. Pino
- Publisher
- John Wiley and Sons
- Year
- 1965
- Tongue
- English
- Weight
- 117 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0044-8249
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✦ Synopsis
Acyl chlorides are split into acyl and chlorine radicals by light of wavelength 254 my. Since the dissociation energy of the chlorine-hydrogen bond is considerably larger than that of the acyl-hydrogen bond, substitution of the substrate by acyl radicals is observed on irradiation of acid chlorides. On irradiation of acetyl chloride the following reactions take place: BrZ CC14 Brz CHCI, BrZ CKCHhCI IC1 CI(CH2)zCI 12 CHCI,
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Thermal reactions of 3-phenyl-5-arylamino-1,2,4-oxadiazoles I and II were investigated. Neat heating at ca. 250ЊC for 6 hours afforded H 2 O, benzonitrile, arylcyanamides, arylamines, azobenzene, benzimidazole derivatives, and 3,3Ј-diphenyl-5,5Ј-bis[1,2,4-oxadiazolyl]. Analogous results were obtaine
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