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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271517Generated: November 3, 2026

Benzyl Alcohol → 2-(Benzyloxy)-4-fluorobenzonitrile

https://huagongshe.com/reaction/1271517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant2,4-DifluorobenzonitrileHCID 77545—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzyloxy)-4-fluorobenzonitrileHCID 2106982839.7%

Reaction Steps

To 2.5 mL benzyl alcohol in 80 mL THF is added 1.87 g NaH. After one hour stirring at room temperature, 5.0 g of 2,4-Difluorobenzonitrile is added. After stirring one hour, the reaction is quenched with excess water and concentrated in vacuo. The residue is redissolved in ethyl acetate and washed with water, brine, dried over sodium sulfate, filtered and concentrated in vacuo. The product is recrystallizde in carbon tetrachloride to give 3.24 g (39.7%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205313B2
Source datasetuspto-grants-2007_04
ORD IDord-85313e45bf884ff39abd94182019d2ff
Source noteuspto-grants-2007_04