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-methoxy-phenyl)-acetic acid (24 g, 97.9 mmol) in ethanol (240 mL) was added thionyl chloride (78 mL, 107.7 mmol) and the reaction was stirred at room temperature for 1.5 hours. Once no starting material was seen by analytical LCMS, saturated sodium bicarbonate (aqueous) was added until the reaction was of basic pH. The mixture was extracted twice with dichloromethane and the combined organic layers were washed with water, dried over magnesium sulfate, filtered, and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785393B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-cb03510f8df548f2841e2bee175e63ce |
| Source note | uspto-grants-2014_07 |