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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610124Generated: October 27, 2026

Pentamethyldiethylenetriamine → 4-Fluoro-3-[(3-fluorophenyl)-hydroxymethyl)-5-methoxybenzonitrile

https://huagongshe.com/reaction/1610124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentamethyldiethylenetriamineHCID 18196—
Reactant3-FluorobenzaldehydeHCID 68009—
Reactant4-Fluoro-3-methoxybenzonitrileHCID 2737365—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Fluoro-3-[(3-fluorophenyl)-hydroxymethyl)-5-methoxybenzonitrileHCID 22260657—

Reaction Steps

To a solution of 15.0 g of 4-fluoro-3-methoxybenzonitrile and 21.8 ml of N,N,N′,N′,N″-pentamethyldiethylenetriamine in 300 ml tetrahydrofuran was added 65.5 ml of a 1.59 M solution of n-butyllithium in hexane at −78° C. in an atmosphere of nitrogen gas, followed by stirring at the same temperature for 1 hour. At the same temperature, 10.5 ml of 3-fluorobenzaldehyde was added dropwise, followed by stirring at the same temperature for 1 hour. Then, water was added and the mixture was extracted with diethyl ether. The organic layer was washed with saturated aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:10 to 1:3), to give 7.1 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982274B2
Source datasetuspto-grants-2006_01
ORD IDord-1da72574d8a7405dae7e4527bd333f7d
Source noteuspto-grants-2006_01