HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 5-(1-hydroxy-2-methylpropan-2-yl)thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(2-Hydroxy-1,1-dimethyl-ethyl)-thiophene-2-carboxylic acid | HCID 67484515 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-(1-hydroxy-2-methylpropan-2-yl)thiophene-2-carboxylate | HCID 67484466 | 83% |
Reaction Steps
A solution of 5-(2-hydroxy-1,1-dimethyl-ethyl)-thiophene-2-carboxylic acid (0.495 g, 2.47 mmol) in DMF (12.0 mL) is treated with K2CO3 (0.515 g, 3.73 mmol), iodomethane (0.23 mL, 3.69 mmol), and stirred at rt overnight. The mixture is poured into H2O (25 mL) and extracted with EtOAc (3×25 mL). The combined extracts are washed with H2O, brine, dried over MgSO4, filtered, and concentrated. The residue is loaded onto silica gel and eluted with hexanes using a gradient of 0% to 75% EtOAc to give 5-(2-hydroxy-1,1-dimethyl-ethyl)-thiophene-2-carboxylic acid methyl ester (0.439 g, 83%). MS (ES): 215.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084489B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-aa43d418331a42d69b5c453c0988f090 |
| Source note | uspto-grants-2011_12 |