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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23519Generated: October 26, 2026

Hydrochloric Acid → 1-(4-Fluorophenyl)-2-(2-fluoropyridin-4-yl)ethanone

https://huagongshe.com/reaction/23519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBenzoic acid, 4-fluoro-, ethyl esterHCID 67976—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant2-Fluoro-4-methylpyridineHCID 2737403—
Product1-(4-Fluorophenyl)-2-(2-fluoropyridin-4-yl)ethanoneHCID 11031769—

Reaction Steps

To a solution of sodium bis(trimethylsilyl)amide (0.465 L, 1M) in TBF (765 mL) under nitrogen, cooled to 2° C., was added 2-fluoro-4-methylpyridine (25 g, 0.225 mol) and the solution stirred for 45 minutes in an ice bath. Ethyl 4-fluoro-benzoate (35 mL, 0.239 mol) was added and the reaction was stirred for 1.5 hours at RT. The reaction mixture was poured into excess aqueous 2N HCl, and the aqueous layer was made basic with 5 N NaOH and extracted with EtOAc. The organic extracts were combined, washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was dissolved in CH2Cl2 and filtered through a cotton plug. Hexanes were added and the CH2Cl2 was removed under reduced pressure until precipitation of the title compound occurred as a pale yellow solid (43.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852727B2
Source datasetuspto-grants-2005_02
ORD IDord-8b2ce258c09b4c8d8cddd43a27d5f774
Source noteuspto-grants-2005_02