HCID 14750997, compound → 2-Aminotetralin

Participants

Reaction Steps

Following the procedure of Example 27, but starting from 4-(2,3-epoxypropoxy)indane (19 g) and 2-aminotetralin (14.81 g) in absolute ethanol (150 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-indan-4-yloxypropanamine hydrochloride is obtained ((iA): E and G, taken together, represent a group --CH2 --CH2 --CH2 --, R=H, and the chain is attached to position 2 of the tetralin moiety).

Provenance & Evidence