HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-chloropropionate → Ethyl 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-chloropropionate | HCID 10807 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-(4-(Trifluoromethyl)phenoxy)phenol | HCID 170230 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Ethyl 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoate | HCID 631921 | 54% |
Reaction Steps
A solution of 73.5 g of 4-(4-trifluoromethylphenoxy)phenol and 49.2 g of ethyl α-chloropropionate and 100 g of potassium carbonate were added to 100 ml of methyl ethyl ketone, and the mixture was heated. With stirring, the reaction was performed for 10 hours at the reflux temperature (80° to 85° C.). Inorganic salts were separated from the reaction product by filtration. The filtrate was evaporated and dried. The resulting ester was extracted with chloroform, and washed with water. The chloroform was distilled off to afford 55 g of the final product (yield: 54%). The final product had a boiling point of 176° to 185° C./3 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309562 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-0180b70e8a9e4fb0a1e4ae74dd24f9d1 |
| Source note | uspto-grants-1982_01 |