HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-Isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Isopropyl-6-(trifluoromethyl)-1H-indole-4-carbonitrile | HCID 67466134 | — |
| Product | 1-Isopropyl-6-(trifluoromethyl)-1H-indole-4-carboxylic acid | HCID 67464224 | 86% |
Reaction Steps
To a solution of 1-(1-methylethyl)-6-(trifluoromethyl)-1H-indole-4-carbonitrile (180 mg, 0.714 mmol) in ethanol (5 mL) was added 10% sodium hydroxide (5 mL, 0.714 mmol), and the mixture was heated at reflux overnight. The mixture was concentrated to remove EtOH and the aqueous phase was acidified using 1N HCl to ˜pH 4. The precipitate was collected by filtration and dried under high vacuum to give the title compound (167 mg, 86%) as brown solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.43-1.60 (m, 6H), 4.96-5.13 (m, 1H), 7.11 (d, J=3.28 Hz, 1H), 7.89-8.05 (m, 2H), 8.25 (s, 1H), 13.15 (br. s., 1H). MS: (M+H)+=272.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09114141B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-d40b90ee68444d6c9adf01ae46f1bf14 |
| Source note | uspto-grants-2015_08 |