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(In connection with the last it may be of some relevance that the compound may be viewed as a ringcontracted analogue of the tricyclic antidepressants.) Reaction of substituted nitrile 46^with phenylmagnesium bromide gives, after hydrolysis, the benzophenone K Reaction of the ketone with the ylide from trimethylsulfoxonium iodide leads to the epoxide 48. Reductive ring opening of the oxirane by means of phosphorus and hydriodic acid completes conversion of the carbonyl to the homologous methyl group (49). Replacement of bromine by a nitrile group is accomplished by treatment of _4S^ with cuprous cyanide. Reaction of the product with the Grignard reagent from 3-methoxybromopropane affords the inline j>l_9 which now contains all the required carbon atoms. Treatment of this intermediate with hybrobromic acid achieves both FriedelCrafts-like ring closure and conversion of the terminal methoxy group to a bromide (52). 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