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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593885Generated: October 30, 2026

Water → 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylic acid

https://huagongshe.com/reaction/593885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylateHCID 67464634—
SolventEthanolHCID 702—
Product6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylic acidHCID 6746867889.9%

Reaction Steps

To a stirred solution of methyl 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylate (24 g, 77.4 mmol) in ethanol (400 mL) was added sodium hydroxide (4.02 g, 100.6 mmol), water (11 mL) and the mixture was stirred at reflux condition for 6 h. Ethanol was distilled off and residue was diluted with water, extracted with ethylacetate (40 mL) adjusted aqueous layer to PH˜3 with 1N HCl and extracted with ethyl acetate (3×250 mL), finally organic layer was washed with brine solution, dried over anhydrous Na2SO4 and concentrated. The crude was washed with pet ether, filtered the solid and dried to afford desired product 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylic acid (20.6 g, 89.8%). 1H NMR (DMSO-d6, 400 MHz): δ 1.407 (d, J=6.4 Hz, 6H), 2.296 (s, 3H), 4.754-4.819 (m, 1H), 7.455 (s, 1H), 7.472 (s, 1H), 7.938 (s, 1H), 12.950 (brs, 1H). LCMS (ES+) m/z=296.15 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242962B2
Source datasetuspto-grants-2016_01
ORD IDord-d95d4b3117de4733ae3bf9814aaf3998
Source noteuspto-grants-2016_01