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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516764Generated: October 30, 2026

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

https://huagongshe.com/reaction/516764

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 numberUS09114141B2
Source datasetuspto-grants-2015_08
ORD IDord-5ef7b295e69445b09e734a7e34f60428
Source noteuspto-grants-2015_08