Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

70093-12-8

2-(4-FLUOROPHENYL)-1H-INDOLE-3-CARBOXAL& synthesis

4synthesis methods
-

Yield:70093-12-8 88%

Reaction Conditions:

Stage #1: 2-(4-fluorophenyl)indolewith N,N-dimethyl-formamide;trichlorophosphate at 10 - 50;
Stage #2: with sodium hydrogencarbonate in water at 60; for 0.25 h;

Steps:

9

1.7 mL of POCl3 was added drop wise to a solution of the 2(4-fluorophenyl)-indole (2.11 g) in 20 mL of DMF, at 10° C. The mixture was stirred at 50° C. for 1 hr, cooled and diluted with saturated NaHCO3. Th e suspension was heated at 60° C. for 15 min, cooled, and the precipitates of 2-(4-fluorophenyl)-indole-3-carboxaldehyde were filtered and crystallized from EtOH. Yield 2.10 g (88%).

References:

US2010/168417,2010,A1 Location in patent:Page/Page column 32-33