HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83680Generated: October 29, 2026
Hydrochloric Acid → 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/83680
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate | HCID 68380121 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylic acid | HCID 68379759 | — |
Reaction Steps
ethyl 1-(4-chlorobenzyl)-7-methyl-1H-indole-2-carboxylate (212 mg, 0.647 mmol) was dissolved in EtOH (10 mL) and 10% aq. KOH (10 mL) was added. The reaction stirred for 4 h at 70° C., after which time as much solvent was stripped off as possible. The mostly aqueous mixture was cooled in an ice bath and acidified with concentrate HCl to obtain a precipitate that was collected over a filter and washed with 1M HCl and water. The title compound was not purified or characterized further. (Yield: 182 mg, 0.607 mmol, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846684B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f4d921ab8ce6418694df645a48989564 |
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| Source note | uspto-grants-2014_09 |
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