HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249652Generated: October 28, 2026
Hydrochloric Acid → 5-(2,4-diisobutoxybenzoyl)-1-isobutyl-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/2249652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 5-(2,4-diisobutoxybenzoyl)-1-isobutyl-1H-indole-2-carboxylate | HCID 17816510 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-(2,4-diisobutoxybenzoyl)-1-isobutyl-1H-indole-2-carboxylic acid | HCID 17816450 | 88.4% |
Reaction Steps
In 2 ml of ethanol is dissolved 0.18 g of ethyl 5-(2,4-diisobutoxybenzoyl)-1-isobutyl-1H-indole-2-carboxylate. After adding 0.3 ml of 5 mol/L sodium hydroxide, the mixture thus obtained is stirred at ambient temperature for one hour. Water and chloroform are added to the reaction mixture, pH is adjusted to 2 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; hexane:ethyl acetate=1:1). Thus, 0.15 g of 5-(2,4-diisobutoxybenzoyl)-1-isobutyl-1H-indole-2-carboxylic acid is obtained as a white solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314888B1 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-c3d994a116404c4d804fa22e8e7115f0 |
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| Source note | uspto-grants-2008_01 |
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