HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-bromo-4-methoxyphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Bromo-4-methoxyphenylacetic acid | HCID 136615 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | Ethyl 3-bromo-4-methoxyphenylacetate | HCID 57419861 | — |
Reaction Steps
To 3-bromo-4-methoxyphenylacetic acid (24 g, 97.9 mmol) in ethanol (240 mL) was added thionyl chloride (7.8 mL, 107.7 mmol), and the reaction was stirred at room temperature for 1 hour. Once no starting material was seen by analytical LCMS, the mixture was basified with saturated aqueous NaHCO3 and extracted with dichloromethane. The combined organic layers were dried over MgSO4, filtered, and concentrated to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440707B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-43a2591ff17d4ad196e9170abcc03b3b |
| Source note | uspto-grants-2013_05 |