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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236371Generated: November 1, 2026

Benzyl Alcohol → 4-Benzyloxy-3,5-difluorobenzonitrile

https://huagongshe.com/reaction/2236371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant3,4,5-TrifluorobenzonitrileHCID 593814—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy-3,5-difluorobenzonitrileHCID 5744572289.7%

Reaction Steps

To a solution of 5.0 g of 3,4,5-trifluorobenzonitrile and 4.5 g of benzyl alcohol in 25 ml of DMF was added 1.5 g of 60% sodium hydride (oily) at 0° C. The mixture was stirred at room temperature for 4 hours. Then, dilute hydrochloric acid was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 7.0 g of 4-benzyloxy-3,5-difluorobenzonitrile represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714168B2
Source datasetuspto-grants-2010_05
ORD IDord-2bcb7f931c734b518f99d895c16d61c1
Source noteuspto-grants-2010_05