Issue 8, 1985

Contributions to the chemistry of boron. Part 160. A convenient synthesis of catecholatoborane and diborane

Abstract

Catecholatoborane is formed in high yield (> 75%) by ball milling NaBH4 and 2,2′-o-phenylene-dioxybis(1,3,2-benzodioxaborole) in diethyl ether in the presence of small amounts of LiCl. It also results quantitatively from the first two components in diglyme (MeOCH2CH2OCH2CH2OMe), but cannot be separated from the solvent. The reaction between NaBH4 and catecholatoborane or the o-phenylene compound in diglyme can also be used to prepare diborane in high yield.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1985, 1689-1692

Contributions to the chemistry of boron. Part 160. A convenient synthesis of catecholatoborane and diborane

D. Männig and H. Nöth, J. Chem. Soc., Dalton Trans., 1985, 1689 DOI: 10.1039/DT9850001689

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