Réaction #3442

ord-5df3c79084144f99bcdc789e25be2a1e

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

By the method used in Example 1, Part D, 1.25 g (3.8 mmol) of 1-([1,1'-biphenyl]-3-ylmethyl)-4-methoxy-2-methyl-1H-indole was O-demethylated by treating it with 15.2 mL of 1M BBr3 /CH2 Cl2 to give 1.03 g (87% yield) of crude 1-([1,1'-biphenyl]-3-ylmethyl)-4-hydroxy-2-methyl-1H-indole.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05733923uspto-grants-1998_03