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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183726Generated: November 2, 2026

Ethyl Acetate → HCID 57995482, compound

https://huagongshe.com/reaction/1183726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium fluorideHCID 25953—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
ReactantHCID 57995511HCID 57995511—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57995482HCID 5799548280.8%

Reaction Steps

A mixture of ethyl 1-(3-chloro-4-iodo-5-(2,2,2-trifluoroethoxy)phenyl)cyclopentanecarboxylate (0.58, 1.2 mmol), 4-trifluoromethylphenylboronic acid (0.56 g, 2.4 mmol), CsF (0.46 g, 3.0 mmol) and Pd (PPh3)4 (0.14 g, 0.12 mmol) in 20 mL anhydrous 1,2-dimethoxy ethane was refluxed for 8 h under argon. The reaction mixture was cooled, and 25 mL of EtOAc and 25 mL of water were added. The organic phase was separated, dried over Na2SO4, filtered and concentrated under reduced pressure to yellow oil. The oil was purified by column chromatography over silica gel (hexane/EtOAc, 95:5) to give ethyl-1-(2-chloro-6-(2,2,2-trifluoroethoxy)-4′-(trifluoromethyl)biphenyl-4-yl)cyclopentanecarboxylate (0.480 g) as a color less oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664249B2
Source datasetuspto-grants-2014_03
ORD IDord-d502b1eb41e441ce986e4660845f15ba
Source noteuspto-grants-2014_03