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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487384Generated: October 31, 2026

Ethyl Acetate → 5-(3,5-Difluorobenzyloxy)nicotinonitrile

https://huagongshe.com/reaction/1487384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant3,5-Difluorobenzyl bromideHCID 518896—
Reactant5-Hydroxypyridine-3-carbonitrileHCID 15342142—
SolventDimethylacetamideHCID 31374—
Product5-(3,5-Difluorobenzyloxy)nicotinonitrileHCID 6827653368%

Reaction Conditions

Temperature0 °C

Reaction Steps

876 mg (2 eq) of sodium hydride is added gradually at 0° C. under nitrogen to a solution of 865 mg of 5-hydroxynicotinonitrile (7.2 mmol) in 15 mL of dimethylacetamide. The mixture is stirred 10 min at 0° C. before adding 2.24 g (1.5 aq) of 3,5-difluorobenzyl bromide. The mixture is placed under stirring for 2.5 additional hours before being diluted in an ethyl acetate fraction and being washed with aqueous fractions. The organic phases are isolated, dried and concentrated. The solid residue obtained is recrystallized in methanol to yield 1.1 g (68% of 5-(3,5-difluorobenzyloxy) nicotinonitrile in the form of a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428510B2
Source datasetuspto-grants-2016_08
ORD IDord-f3fcfa34abe94d0099b5846281a462be
Source noteuspto-grants-2016_08