Synthesis of 25-Hydroxy-provitamin D₃ by Direct Hydroxylation of Protected 7-Dehydrocholesterol

Abstract

A new synthetic route to 25-hydroxy-provitamin D 3 was elaborated. The synthesis consists of direct hydroxylation at C-25 of 7-dehydrocholesterol hetero Diels−Alder adducts. The adducts were prepared by [4 + 2] cycloaddition of azadienophiles to the steroidal diene. The hydroxylation reactions of adducts were carried out with different dioxiranes or with chromyl trifluoroacetate. The byproducts of these reactions were isolated and identified. The strengths and weaknesses of hydroxylation methods with different oxidizing agents were discussed.