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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727344Generated: November 1, 2026

Water → 2-(2-Fluoro-4-pyridyl)-1-(3-methylphenyl)ethanone

https://huagongshe.com/reaction/1727344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylamineHCID 7912—
Reactant2-Fluoro-4-methylpyridineHCID 2737403—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Fluoro-4-pyridyl)-1-(3-methylphenyl)ethanoneHCID 1154315752%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under an argon atmosphere, a solution of diisopropylamine (44 mL, 0.31 mol) in anhydrous tetrahydrofuran (300 mL) was cooled to −78° C., and to this was added dropwise a 1.6 M n-butyllithium hexane solution (190 mL, 0.31 mol) with stirring. After completion of the addition, the solution was stirred for 10 minutes, subsequently, a solution of 2-fluoro-4-methylpyridine (34.5 g, 0.31 mol) in anhydrous tetrahydrofuran (30 mL) was added. The reaction mixture was stirred for 30 minutes at −10° C. The reaction solution was cooled to −78° C., and a solution of N-(3-methylbenzoyl)propyleneimine (52 g, 0.30 mol) in anhydrous tetrahydrofuran (30 mL) was added dropwise. After completion of the addition, the mixture was stirred for 2 hours at room temperature. To the reaction mixture was added water (100 mL), and extracted with ethyl acetate. The extracted solution was washed with water, dried, then, the solvent was distilled off. The residue was recrystallized from isopropyl ether to obtain a title compound (35 g, yield 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495018B2
Source datasetuspto-grants-2009_02
ORD IDord-bbd2c0efbfb9483888e56ff24a6de0f5
Source noteuspto-grants-2009_02