HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-chloro-5-trifluoromethoxyphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Chloro-5-(trifluoromethoxy)phenylacetic acid | HCID 21904638 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 3-chloro-5-trifluoromethoxyphenylacetate | HCID 21904618 | 96% |
Reaction Steps
To a solution of 3-chloro-5-trifluoromethoxyphenylacetic acid (5.2 g, 20.4 mmol; see step (iii) above) in EtOH (600 mL) was added sulfuric acid (several drops). The solution was refluxed for 18 h, cooled to room temperature, neutralized with solid NaHCO3 and the EtOH removed in vacuo. The residue was diluted with EtOAc then washed with H2O (1×), aqueous NaHCO3 (1×) and brine (1×). The organics were dried (Na2SO4), filtered and concentrated in vacuo to afford the sub-title compound (5.5 g, 96%) as an oil which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129233B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-b21c718078574387a5669f898ea7cfaf |
| Source note | uspto-grants-2006_10 |