HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-chloro-4-hydroxyphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Chloro-4-hydroxyphenylacetic acid | HCID 118534 | — |
| Product | Ethyl 3-chloro-4-hydroxyphenylacetate | HCID 11031224 | — |
Reaction Steps
To an ice-cooled solution of 3-chloro-4-hydroxyphenyl-acetic acid (10.0 g, 53 mmol) in ethanol was dropwise added thionyl chloride (3.9 mL. 53.5 mmol). The mixture was stirred at room temperature over night, concentrated in vacuo and submitted to flash chromatography (eluent: graduated from 10% ethyl acetate in toluene to toluen) to give 11 g of 3-chloro-4-hydroxyphenyl-acetic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06869967B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-e2c860c191e544f3b7fccf9ceb0f6f2c |
| Source note | uspto-grants-2005_03 |