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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301212Generated: October 30, 2026

Ethyl Acetate → HCID 18371303, compound

https://huagongshe.com/reaction/2301212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 18371303HCID 18371303—

Reaction Conditions

Temperature80 °C

Reaction Steps

1.75 g (0.01 mole) of 3-chloro-4-fluoronitrobenzene and 0.013 mole of phenylboric acid were dissolved in 70 mL of 1,2-dimethoxyethane under argon. Then, 0.5 g (0.0005 mole) of tetrakis(triphenylphosphine)palladium and 13 mL of 2N potassium carbonate solution were added, and the reaction mixture was heated to 80° C. At the end of the reaction, the reaction mixture was poured into 100 mL of ethyl acetate. The organic phase was extracted with dilute sodium hydroxide solution and then dried over magnesium sulfate. The solvent was distilled off from a rotary evaporator, and the residue was purified [by column chromatography] on silica gel using hexane/toluene (10:1) [as the eluent].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500213B1
Source datasetuspto-grants-2002_12
ORD IDord-e286b5fdf7764fbf82f7f4656e0f3e54
Source noteuspto-grants-2002_12