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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038348Generated: October 31, 2026

Hydrochloric Acid → 1-Bromo-4-cyano-3-methoxy-5-(4-ethyl-benzyl)-benzene

https://huagongshe.com/reaction/1038348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-2,6-difluorobenzonitrileHCID 2756916—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantEthyl 2-(4-ethylphenyl)acetateHCID 53419404—
SolventMethanolHCID 887—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-Bromo-4-cyano-3-methoxy-5-(4-ethyl-benzyl)-benzeneHCID 58385818—

Reaction Steps

KOtBu (11.8 g) is added to a flask charged with a stir bar and dry NMP (40 mL) and chilled to −10° C. under argon atmosphere. A solution of ethyl (4-ethyl-phenyl)-acetate (10.1 g) and 1-bromo-4-cyano-3,5-difluoro-benzene (11.5 g) in NMP (40 mL) is added at such a rate that the reaction temperature maintains below 10° C. After stirring for 1 hour at room temperature, methanol (50 mL) and 1 M aqueous sodium hydroxide solution (39 mL) are added and the resulting mixture is stirred overnight at 100° C. Then, 4 M aqueous hydrochloric acid (100 mL) is added and the mixture is stirred for another h at 100° C. The methanol fraction is evaporated, water (200 mL) is added to the residue and the resulting mixture is extracted with ethyl acetate. The combined organic extracts are washed twice with water, twice with brine and dried (MgSO4). The solvent is evaporated and the residue is washed with methanol. The insoluble residue is separated by filtration and dried to give the white product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551957B2
Source datasetuspto-grants-2013_10
ORD IDord-a8f6ea36c3b442f6849ce241222ea0ea
Source noteuspto-grants-2013_10