作者:Bojan Hamlin Jennings、Joan Marie Bengtson
DOI:10.1016/0039-128x(78)90019-3
日期:1978.1
5-epoxy-5beta-androstan-3-one (1b) and 17beta-acetoxy-4beta,5-epoxy-5beta-androstan-3-one (1c) were treated with anhydrous hydrogen fluoride in pyridine (70% solution) at 55 detrees and yielded the corresponding 4-en-4-ols, e.g. 4-hydroxy-4-androstene-3,17-dione (2a). As the reaction temperature was lowered each epoxide formed a second product which, at -75 degrees, was the major component of the reaction mixture
4beta,5-epoxy-5beta-androstane-3,17-dione(1a),17beta-hydroxy-4beta,5-epoxy-5beta-androstan-3-one(1b)和17beta-acetoxy-4beta,5-epoxy-在吡啶中(70%的溶液)在无水氟化氢中用吡啶(70%溶液)处理5beta-androstan-3-one(1c),得到相应的4-en-4-ols,例如4-hydroxy-4-androstene-3,17 -二酮(2a)。随着反应温度降低,每个环氧化物形成第二种产物,该产物在-75度下是反应混合物的主要成分,被鉴定为母体烯酮的5α-氟-4α-醇衍生物,例如4α-羟基- 5-氟-5α-雄烷-3,17-二酮(3a)。这些氟代醇是热不稳定的,会损失氟化氢。还制备,表征了氟代氟代醇的乙酸酯,并显示出比母体醇更稳定。