HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-cyano-1H-indole-2-carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 5-cyanoindole-2-carboxylate | HCID 4714953 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-cyano-1H-indole-2-carboxylic Acid | HCID 7144625 | — |
Reaction Steps
5-Cyano-1H-indole-2-carboxylic acid ethyl ester (1.71 g, 8.0 mmol) was added to a solution of ethanol (10 mL) and potassium hydroxide (2 g) and the resulting mixture heated at reflux for 1 hour. Water was added to dissolve the precipitate, and 6N HCl was added to bring the pH to 1. A precipitate formed. The mixture was cooled in an ice bath, filtered, and the resulting colorless solid washed with cold water and dried (1.51 g). A portion (1.4 g) was suspended in hot acetic acid (40 mL) and cooled giving a solid which was filtered, washed with cold ethyl acetate and dried: Yield 980 mg 70%; HPLC (60/40) 3.09 minutes (97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06649634B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-25912878a990425c9d20026f53177011 |
| Source note | uspto-grants-2003_11 |