Reaction #459590

ord-cf5250d885204937873b7a769b29e7e2

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

The process of Example 1 was repeated using 196.2 parts of piperidine in place of the morpholine. The product was the corresponding piperidino enamine which was reacted with benzoquinone in toluene to give 2,3-dihydro-3,3-dimethyl-5-hydroxy-2-piperidino-benzofuran. This was converted to 2,3-dihydro-3,3-dimethyl-2-piperidino-benzofuran-5-yl methanesulphonate and then to 2,3-dihydro-3,3-dimethyl-2-ethoxy-benzofuran-5-yl methane sulphonate as in Example 5.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04091033uspto-grants-1978_05