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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65393Generated: October 29, 2026

Potassium Carbonate → 2-Benzylthioethyl 2-[4-(5-trifluoromethyl-2-pyridyloxy)-phenoxy]-propionate

https://huagongshe.com/reaction/65393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
Reactant2-(Benzylsulfanyl)ethyl 2-(4-hydroxyphenoxy)propanoateHCID 13309629—
SolventDimethyl SulfoxideHCID 679—
Product2-Benzylthioethyl 2-[4-(5-trifluoromethyl-2-pyridyloxy)-phenoxy]-propionateHCID 1330947376.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

15.2 g of potassium carbonate were added to a solution of 33.2 g of 2-benzylthioethyl 2-(4-hydroxyphenoxy)-propionate in 100 ml of dimethyl sulfoxide at room temperature whilst stirring. The mixture was heated to 90° C. for 1 hour with stirring. Then, 20.0 g of 2-chloro-5-trifluoromethyl-pyridine were added thereto while maintaining the temperature between 80° and 90° C. After the addition was completed, the reaction mixture was further stirred at this temperature for 2 hours, and then cooled to room temperature. Then the reaction mixture was poured into ice water and extracted with chloroform. After drying the organic phase, the chloroform was removed under reduced pressure. There were obtained 36.3 g of 2-benzylthioethyl 2-[4-(5-trifluoromethyl-2-pyridyloxy)-phenoxy]-propionate in the form of a pale yellow viscous oil. nD20 =1.5505.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614536
Source datasetuspto-grants-1986_09
ORD IDord-c92cc25d9a3f409c9b8e459df009c1c6
Source noteuspto-grants-1986_09