HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449087Generated: October 25, 2026
Sodium Hydroxide → 2-[(1-Ethyl-2-methyl3-indolyl)carbonyl]-5-aminobenzoic acid
https://huagongshe.com/reaction/1449087
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(1-Ethyl-2-methyl-1H-indole-3-carbonyl)-5-nitrobenzoic acid | HCID 20523561 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2-[(1-Ethyl-2-methyl3-indolyl)carbonyl]-5-aminobenzoic acid | HCID 20523566 | 54.3% |
Reaction Steps
To a solution of 7.04 g (0.02 mole) of 2-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-5-nitrobenzoic acid, prepared as described in part A of this example, in 70 ml of concentrated hydrochloric acid, there was added 13.5 g (0.06 mole) of stannous chloride dihydrate at such a rate as to allow the reaction to exotherm to 55° C. The temprature was maintained at 55° C. for an additional one-half hour. The reaction was then cooled to room temprature and the pH adjusted to six by the addition of 10 percent aqueous sodium hydroxide solution. The red precipitate thus formed was filtered off and extracted into acetone. The acetone solution was evaporated and the paste-like residue was slurried in diethylether and then the solid was collected by filtration to obtain 3.5 g of 2-[(1-ethyl-2-methyl-3-indolyl)-carbonyl]-5-aminobenzoic acid (Formula VIII: R3 =R2 =R°=Y1 =H; R1 =NH2 ; R5 =CH3 ; R6 =CH2CH3), a red solid which melted at 187°-189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04189171 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-8c9fc533165242f482b94dbf62eed45f |
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| Source note | uspto-grants-1980_02 |
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