A study of the reactions involved in the preparation of 16α‐methyl‐17α‐hydroxy‐21‐acetoxy‐Δ1;4;9,11‐pregnatriene‐3, 20‐dione (V) from the corresponding 11α‐sulfonyloxy‐2,4‐dibromo‐allopregnane‐3,20‐diones led to a process in which all three substituents in 2‐, 4‐ and 11α‐positions are eliminated simultaneously. 2‐Halogen‐Δ4;9,11‐pregnadiene‐3,20‐diones were formed as by‐products which were reduced to the halogen‐free dienes.
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Wieland et al. (1960) studied this question.
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