HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-bromothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Bromo-2-thiophenecarboxylic Acid | HCID 610409 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-bromothiophene-2-carboxylate | HCID 10847330 | — |
Reaction Steps
663 mg (3.20 mmol) of the compound from Example 6A are provided in 25 ml of ethanol, 0.1 ml of concentrated sulfuric acid is added and the mixture is heated under reflux overnight. After cooling to room temperature, a saturated aqueous sodium bicarbonate solution is added and the mixture is diluted with water and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated. 700 mg (89% of theory) of the title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546438B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-96a238aeec2a4734962534341646e20c |
| Source note | uspto-grants-2013_10 |