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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylate | HCID 67464634 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylic acid | HCID 67468678 | 89.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242962B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-d95d4b3117de4733ae3bf9814aaf3998 |
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| Source note | uspto-grants-2016_01 |
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