HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988143Generated: October 25, 2026
Water → 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid
https://huagongshe.com/reaction/988143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Reactant | 5-(1H-indol-4-yl)-nicotinic acid | HCID 22135477 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid | HCID 22135397 | 98% |
Reaction Steps
Pyridinium tribromide (90% (Aldrich), 9.8 g, 27.6 mmol) was added portion-wise over 10 minutes to a suspension of 5-(1H-indol-4-yl)-nicotinic acid (2.2 g, 9.2 mmol) in 2-methyl-2-propanol (54 mL), ethanol (36 mL) and acetic acid (108 mL). The mixture was stirred at room temperature for 2 hours and then acetic acid (10 mL) was added. After stirring for an additional hour, water (0.5 mL) and zinc dust (6 g, 92 mmol) were added and stirring was continued for another hour. Residual zinc dust was filtered and washed with methanol. The filtrate was concentrated and the syrupy residue was stirred in water (300 mL) overnight. The solid which formed was filtered, washed with water to remove zinc and pyridine salts and dried under high vacuum to give 2.3 g (98%) of 5-(2-oxo-2,3-dihydro-1H-indol-4-yl)-nicotinic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06635640B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-4f0f685df7fb4da1ba4fe72076fc25ec |
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| Source note | uspto-grants-2003_10 |
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