HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276126Generated: October 30, 2026
Hydrochloric Acid → HCID 12051604, compound
https://huagongshe.com/reaction/276126
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13186946 | HCID 13186946 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12051604 | HCID 12051604 | — |
Reaction Steps
A stirred mixture of ethyl 4-oxo-6-methyl-4,5,6,7-tetrahydrobenzofuran-3-carboxylate (15.7 g, 71 mmol) and ammonium acetate (9.54 g, 124 mmol) in N,N,-dimethylformamide (75 mL) was heated at 100° C. for 2 hours. The reaction mixture was concentrated in vacuo, ice water was added, and the precipitate collected, rinsed with water then diethyl ether and dried to give ethyl 4-oxo-6-methyl-4,5,6,7-tetrahydro-1H-indole-3-carboxylate (5.94 g). To this ester was added aqueous 5N sodium hydroxide (50 mL) and ethyl alcohol (10 mL) and the mixture heated at reflux for 40 minutes. The reaction mixture was cooled in an ice water bath, acidified with aqueous hydrochloric acid, and the precipitate collected, rinsed with water then diethyl ether and dried to give 4-oxo-6-methyl-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (5.2 g). m.p. 210-211° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353109B2 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-87cab5ec4b3e4d2897d98bb5d12ceb69 |
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| Source note | uspto-grants-2002_03 |
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