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Hetero-Cope rearrangement for the synthesis of potassium 5-tert-butyl-2-(tert-butyl-aminoxy)-benzoate, a highly water-soluble stable free radical

✍ Scribed by Lucien Marx; André Rassat


Book ID
104250735
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
59 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


The hetero-Cope rearrangement of 4-tert-butyl-phenyl-tert-butylhydroxylamine provides an easy access to the corresponding ortho-bromoaniline, converted to the new highly water-soluble nitroxide, potassium 5-tert-butyl-2-(tert-butyl-aminoxy)benzoate. The parent carboxylic acid was found to be very persistent in water at pH 1.