Formation of secondary alcohols in the free radical decomposition of aldehydes

FF Rust, FH Seubold, WE Vaughan

Index: Rust; Seubold; Vaughan Journal of the American Chemical Society, 1948 , vol. 70, p. 4254

Full Text: HTML

Citation Number: 14

Abstract

In an attempt to effect the acetonitrile-diisobutene reaction'in cold concentrated sulfuric acid it has been observed that dimethylneopentylcarbinol is formed SLS the principal product. The expected Nt-octylacetamide, which is produced in good yield in aceticsulfuric acid solution, appears in much diminished amount. In 92% sulfuric acid the yield of the carbinol reaches 70% of the calculated value without formation of hydrocarbon polymer. However, ...

Related Articles:

Poly (oligothiophene-alt-benzothiadiazole) s: tuning the structures of oligothiophene units toward high-mobility “black” conjugated polymers

[Yue, Wei; Zhao, Yun; Shao, Shuyan; Tian, Hongkun; Xie, Zhiyuan; Geng, Yanhou; Wang, Fosong Journal of Materials Chemistry, 2009 , vol. 19, # 15 p. 2199 - 2206]

Synthesen von trail??Pheromonen der Pharaoameise (Monomorium pharaonis (L.))

[Schmitz; Sonnenschein; Gruendemann Journal fur Praktische Chemie, 1980 , vol. 322, # 2 p. 261 - 272]

Organoboranes. 41. Reaction of organoboranes with (dichloromethyl) lithium. Scope and limitations. Synthesis of homologated primary and secondary alcohols

[Brown, Herbert C.; Imai, Toshiro; Perumal, P. Thirumali; Singaram, Bakthan Journal of Organic Chemistry, 1985 , vol. 50, # 21 p. 4032 - 4036]

Fragmentation reactions of optically active trisubstituted cyclopropylcarbinyl radicals

[Hughes,R.J. et al. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1977 , p. 1172 - 1176]

More Articles...