HCID 14750993, compound → 2-Aminotetralin

Participants

Reaction Steps

Following the procedure of Example 27, but starting from 8-(2,3-epoxypropoxy)-2H-chromene (20.4 g) and 2-aminotetralin (14.85 g) in absolute ethanol (120 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2H-chromen-8-yloxy)-propanamine hydrochloride is obtained ((i): R=H, Ar=radical 44, and the chain is attached to position 2 of the tetralin moiety).

Provenance & Evidence