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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100612Generated: October 31, 2026

Dichloromethane → N,N,4-Triethyl-2-fluorobenzamide

https://huagongshe.com/reaction/2100612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-N,N-diethyl-2-fluorobenzamideHCID 24694026—
ReactantHCID 178418750HCID 178418750—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN,N,4-Triethyl-2-fluorobenzamideHCID 6905555888%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-bromo-N,N-diethyl-2-fluorobenzamide (5.12 g, 18.9 mmol) in 100 mL of DMF was added potassium carbonate (6.45 g, 46.7 mmol) and diethylzinc (25.5 mL of a 1.1 M solution in toluene, 28.02 mmol). The solution was degassed with a stream of argon and then there was added [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (1:1) (305 mg, 0.37 mmol). The reaction mixture was allowed to stir at 80° C. for 3 h. The reaction mixture was allowed to cool and was diluted with ethyl acetate. The organics were washed with water and brine, dried (MgSO4) and concentrated. The residue was purified (ISCO, elution with 0-40% EtOAc/hexane, 40 min) to afford 3.70 g (88%) of the title compound as a colorless oil. LRMS (ESI): 224.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572805B2
Source datasetuspto-grants-2009_08
ORD IDord-95297d6ca93c47a59f8ec56740b21ebb
Source noteuspto-grants-2009_08