Oxidation of hindered phenols. V. The 2, 6-di-t-butyl-4-isopropyl and-4-sec-butylphenoxy radicals

CD Cook, BE Norcross

Index: Cook; Norcross Journal of the American Chemical Society, 1956 , vol. 78, p. 3797

Full Text: HTML

Citation Number: 69

Abstract

Preparation of 2, 6-Di-t-butyl-4-isopropylphenol (Ia).-. 4 solution of 60 g.(0.44 mole) of p- isopropylphenol in 50 inl. of benzene was alkylated with isobutylene at 50-60" using 2 ml. of concd. sulfuric acid as the catalyst. 8 After rl. weight gain of 60-65 g.(1.07-1.15 moles) of isobutylene the solution was washed once with water, once with 10% sodium hydroxide and three times with Claisen solution (a 50% potassium hydroxide solution diluted with an ...

Related Articles:

Steric Hindrance as a Factor in the Alkylation of Ambident Anions: The Alkylation of Potassium 2, 6-Di-t-butylphenoxide1, 2

[Kornblum,N.; Seltzer,R. Journal of the American Chemical Society, 1961 , vol. 83, p. 3668 - 3671]

Peroxy esters. 8. Base-catalyzed rearrangement of peroxy esters: formation of alkoxyacetic acid derivatives

[Nishinaga, Akira; Nakamura, Koichi; Matsuura, Teruo Journal of Organic Chemistry, 1983 , vol. 48, # 21 p. 3696 - 3700]

Oxidation of hindered phenols. VII. Solvent effects on the disproportionation of certain phenoxy radicals

[Cook; Norcross Journal of the American Chemical Society, 1959 , vol. 81, p. 1176,1178]

Oxidation of hindered phenols. VII. Solvent effects on the disproportionation of certain phenoxy radicals

[Cook; Norcross Journal of the American Chemical Society, 1959 , vol. 81, p. 1176,1178]

Oxidation of hindered phenols. VII. Solvent effects on the disproportionation of certain phenoxy radicals

[Cook; Norcross Journal of the American Chemical Society, 1959 , vol. 81, p. 1176,1178]

More Articles...