HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615544Generated: October 25, 2026
Potassium Carbonate → 2-(4-Chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionate
https://huagongshe.com/reaction/615544
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-(4-(Trifluoromethyl)phenoxy)phenol | HCID 170230 | — |
| Reactant | 2-{[(4-Chlorophenyl)methyl]sulfanyl}ethyl 2-bromopropanoate | HCID 13309632 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(4-Chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionate | HCID 13309605 | 90.9% |
Reaction Steps
A mixture consisting of 25.4 g of 4-(4-trifluoromethylphenoxy)phenol, 14.5 g of anhydrous potassium carbonate, 33.8 g of 2-(4-chlorobenzylthio)ethyl 2-bromopropionate and 150 ml of dry acetonitrile was refluxed for 3 hours with vigorous stirring. After cooling the reaction mixture to room temperature, the acetonitrile was removed under reduced pressure. Then, 150 ml of toluene were added to the residue and the resulting mixture was washed successively with 1% strength by weight aqueous sodium hydroxide solution and water, followed by dehydration. Upon distilling off the toluene under reduced pressure, there were obtained 46.4 g of 2-(4-chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionate in the form of a colorless oil. nD20 =1.5555.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04500346 |
|---|
| Source dataset | uspto-grants-1985_02 |
|---|
| ORD ID | ord-47c941f55a7b4a46a403978b89ccb1da |
|---|
| Source note | uspto-grants-1985_02 |
|---|