1H-Indole-2-carboxylic acid, 6-chloro-7-fluoro- synthesis

Yield:259860-07-6 98%

Reaction Conditions:

with sodium hydroxide in tetrahydrofuran;

Steps:

10 6-Chloro-7-fluoroindole-2-carboxylic Acid

6-Chloro-7-fluoroindole-2-carboxylic Acid A stirred solution of methyl 6-chloro-7-fluoroindole-2-carboxylate (2.3 g, 10 mmol), tetrahydrofuran (20 mL) and aqueous sodium hydroxide solution (2 N, 20 mL) was heated under reflux for 16 h. The mixture was cooled to room temperature and partitioned between aqueous sulfiuric acid (2 M, 30 mL) and ethyl acetate (3*30 mL). The combined organic extracts were dried (magnesium sulfate) and concentrated in vacuo to give the product (2.1 g, 98% yield) as a white solid: IR ν_max (Nujol)/cm^-1 1681, 1557, 1263, 1206, 926 and 840; NMR δ_H (400 MHz, DMSO-d₆) 7.01-7.12 (2H, m) and 7.31-7.34 (1H, m).

References:

US6380238,2002,B1