HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-cyano-3-iodo-5-(methylthio)thiophene-2-carboxylate | HCID 40152061 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid | HCID 58022862 | 80% |
Reaction Steps
To a solution of ethyl 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylate (3.40 g, 10 mmol) in tetrahydrofuran (80 mL) and water (16 mL) was added a solution of 1.00M sodium hydroxide in water (30 mL). The solution was allowed to stir overnight. The reaction was quenched with a solution of 1N hydrogen chloride in water (50 mL) and diluted with water (400 mL). The resultant precipitate was filtered, washed with water (2×100 mL) and dried in a vacuum oven to give 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.6 g, 79%) as a white solid. LCMS: (FA) ES+ 326. 1H NMR (400 MHz, d6-DMSO) δ: 14.1-13.8 (bs, 1H), 2.75 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440664B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-2f4aef9ef39547699a17f8baf8bb12c3 |
| Source note | uspto-grants-2013_05 |