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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494137Generated: November 2, 2026

Lithium Chloride → Ethyl [3-(pyridin-3-yl)phenyl]acetate

https://huagongshe.com/reaction/1494137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
ReactantHexamethylditinHCID 6327618—
Reactant3-Pyridyl TrifluoromethanesulfonateHCID 11031579—
ReactantHCID 14986694HCID 14986694—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl [3-(pyridin-3-yl)phenyl]acetateHCID 14986695—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2.04 g (6.5 mmol) of ethyl m-(trifluoromethanesulfonyloxy)phenylacetate in 33 mL dioxane is added 1.33 mL (6.5 mmol) hexamethylditin followed by 1.49 g (6.6 mmol) 3-(trifluoromethanesulfonyloxy)-pyridine, 0.827 g (19.5 mmol) lithium chloride and 0.15 g (0.13 mmol) tetrakis-(triphenylphosphine) palladium(0). The mixture is then heated at 90° C. for 62 hours, diluted with ether and washed with 10% ammonium hydroxide followed by water and brine. The organic layer is dried, filtered, evaporated and the residue is purified by flash chromatography using 1:1 ether and hexane as eluent to give ethyl m-(3-pyridyl)phenylacetate; IR (CH2Cl2) 1731 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-4683e9a3b3364fceb1397758c537615f
Source noteuspto-grants-1991_06