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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467983Generated: October 30, 2026

Cesium carbonate → (6-Trifluoromethyl-pyridin-2-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/467983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantAmmonium ChlorideHCID 25517—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant2-Bromo-6-(trifluoromethyl)pyridineHCID 2782902—
Reactant2,2-DiethylpropanedioateHCID 6951563—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(6-Trifluoromethyl-pyridin-2-yl)-acetic acid ethyl esterHCID 58216744—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of caesium carbonate (1.87 g, 5.75 mmol) and tri-t-butylphosphine (107 μL, 0.44 mmol) in dry 1,2 dimethoxyethane (10 mL) was treated with tris-(dibenzylideneacetone)di-palladium (81 mg, 0.09 mmol), 2-Bromo-6-(trifluoromethyl)pyridine (1 g, 4.42 mmol) and diethylmalonate (0.8 mL, 5.3 mmol) under nitrogen atmosphere. The mixture was heated to 150° C. for 30 min in a microwave oven. After cooling to 20° C. the mixture was treated with a saturated solution of ammonium chloride (120 mL) and extracted with ethyl ether (3×80 mL). The organic phase was dried and evaporated to give a crude oil that was purified by flash chromatography eluting with n-hexane/ethyl ether 6/1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623901B2
Source datasetuspto-grants-2014_01
ORD IDord-324094b410cd4a10b7af947ebfe95bd2
Source noteuspto-grants-2014_01