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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807856Generated: October 30, 2026

Triethylamine → HCID 21075354, compound

https://huagongshe.com/reaction/1807856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant1,3-Bis(diphenylphosphino)propaneHCID 81219—
Reactant1-bromo-4-fluoro-2-(methoxymethyl)benzeneHCID 2769414—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 21075354HCID 21075354—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under an argon atmosphere, to a solution of 3.45 g of 1-bromo-4-fluoro-2-(methoxymethyl)benzene in 20 mL of dimethylsulfoxide were added 353 mg of palladium acetate, 650 mg of 1,3-bis(diphenylphosphino)propane, 4.4 mL of triethylamine, and 10 mL of methanol in this order, and the atmosphere in the reaction container were replaced with carbon monoxide, followed by stirring at 70° C. for 6 hours. The reaction mixture was poured into a mixed liquid of water and ethyl acetate. The aqueous layer was separated, the organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (normal hexane/ethyl acetate) to obtain 1.75 g of methyl 4-fluoro-2-(methoxymethyl)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357688B2
Source datasetuspto-grants-2013_01
ORD IDord-f50bdf6dd6264dd09309f3bab55a16d0
Source noteuspto-grants-2013_01