HEXACHLOROACETONE is very readily reduced to hexachloroisopropanol by I-benzyl-l,f+-dihydronicotinamide. The reduction goes violently at room and is accompanied went vigorously. temperature in the absence of solvent, is exothermic, by formation of a black tar. Even at 0' the reaction cc13cocc13 + HC
Mechanism of reduction of benzylidenemalononitrile by 1-benzyl-1,4-dihydronicotinamide
โ Scribed by Hong-Yi Wang; You-Cheng Liu; Xiao-Qing Zhu; Qing-Xiang Guo
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 250 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0256-7660
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02139 (R8ceived in IJR 12 Cctober 1972; acoepted for publication 26 Octobar 1972) le would like to report the dimerization of I-benzyl-1,4-dihydronicotinamide in acidic aqueous suspension to form the polycyclic cage molecule 1 in high yield. Although