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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615546Generated: October 30, 2026

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

https://huagongshe.com/reaction/615546

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 numberUS04500346
Source datasetuspto-grants-1985_02
ORD IDord-b3fa918ebcc94a8ab61fdd8e50a288d3
Source noteuspto-grants-1985_02