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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508421Generated: October 31, 2026

Triethylamine → Methyl 5-chloro-2-fluoro-4-methylbenzoate

https://huagongshe.com/reaction/508421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Bromo-2-chloro-5-fluorotolueneHCID 2736228—
ReactantHCID 178418416HCID 178418416—
SolventMethanolHCID 887—
ProductMethyl 5-chloro-2-fluoro-4-methylbenzoateHCID 5804251393%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-bromo-5-chloro-2-fluoro-4-methylbenzene (Comm, 10 g, 44.7 mmol) in methanol (200 mL) was added 1,1′-binaphthalene-2,2′-diylbis(diphenylphosphine)-dichloropalladium (1:1) (358 mg, 0.447 mmol) and N,N-diethylethanamine (8.11 mL, 58.2 mmol). The resulting mixture was placed in a bomb and pressurized with carbon monoxide to 80 psi and heated at 80° C. for 18 hours. The reaction mixture was then concentrated in vacuo to yield a semi-solid, which was dissolved in EtOAc (300 mL) and washed with water (200 mL). The organic layer was separated, dried over magnesium sulphate, filtered and concentrated in vacuo to yield an orange oil, which solidified on standing (9.87 g). The solid was purified by silica gel chromatography eluting with 0 to 20% EtOAc in heptane to afford the title compound as a crystalline white solid (8.47 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096500B2
Source datasetuspto-grants-2015_08
ORD IDord-e9c5bcda29134b399834cabad3a11163
Source noteuspto-grants-2015_08