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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267979Generated: October 30, 2026

Hydrochloric Acid → 2-(3,5-Difluorophenyl)-5-pentylpyrimidine

https://huagongshe.com/reaction/2267979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-3,5-difluorobenzeneHCID 136313—
ReactantMagnesiumHCID 5462224—
Reactant2-Chloro-5-pentylpyrimidineHCID 16756526—
CatalystNickel DichlorideHCID 24385—
SolventTetrahydrofuranHCID 8028—
Product2-(3,5-Difluorophenyl)-5-pentylpyrimidineHCID 1834827015.4%

Reaction Steps

Grignard reagent was prepared from dried magnesium and 49.0 g (254 mmol) of 3,5-difluorobromobenzene in 200 ml of tetrahydrofuran (THF), 1 g of NiCl2 (dppp) was added thereto, 36.0 g (195 mmol) of the 2-chloro-5-pentylpyrimidine described above was added dropwise thereto, and the product was heated to reflux for 2 hours. The reaction solution was cooled down, and added into 200 ml of 1N-hydrochloric acid. The product was extracted with ether, and the extract was washed with saturated aqueous solution of sodium bicarbonate and water in turn, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure. The residue was purified by silica gel column chromatography (eluent: heptane/toluene=1/1) to obtain 8.0 g (30 mmol) of 2-(3,5-difluorophenyl)-5-pentylpyrimidine. Yield of this product was 15%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326065B1
Source datasetuspto-grants-2001_12
ORD IDord-2ff8042a9d594a9287bcec7bd91a2a0a
Source noteuspto-grants-2001_12