HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-(Trifluoromethyl)Thiazole-5-Carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Thiazolecarboxylic acid, 4-(trifluoromethyl)-, ethyl ester | HCID 13593399 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Trifluoromethyl)Thiazole-5-Carboxylic Acid | HCID 18943373 | 99.1% |
Reaction Steps
An aqueous sodium hydroxide solution (2 ml) was added to a solution of ethyl 4-(trifluoromethyl)-1,3-thiazole-5-carboxylate (301 mg) in ethanol (3 ml), followed by stirring at room temperature for 4 hours. The reaction solution was concentrated under reduced pressure and water was added thereto, followed by washing with diethylether. A 1M hydrochloric acid (2 ml) was added to the aqueous layer, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to obtain 4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid (261 mg) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377923B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-901215f9323249abad37b22f8e7bd8ca |
| Source note | uspto-grants-2013_02 |