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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087715Generated: November 1, 2026

Hydrochloric Acid → 3-(2-Methoxybenzoyl)benzonitrile

https://huagongshe.com/reaction/1087715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant2-BromoanisoleHCID 11358—
Reactant3-Cyanobenzoyl chlorideHCID 308483—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Methoxybenzoyl)benzonitrileHCID 1571853380%

Reaction Conditions

Temperature-75 °C

Reaction Steps

30 g (0.16 mol) of 2-bromoanisole are added dropwise to a mixture of 3.85 g (0.16 mol) of magnesium, containing a crystal of iodine, in 75 ml of anhydrous tetrahydrofuran and the reaction mixture is then refluxed for 1 hour. The resulting solution is then added dropwise to a solution of 26.48 g (0.16 mol) of 3-cyanobenzoyl chloride in 75 ml of anhydrous tetrahydrofuran, cooled to -75° C. The temperature is allowed to rise to 20° C., the reaction medium is hydrolyzed with a 1N aqueous solution of hydrochloric acid and the expected product is then extracted with ethyl acetate. The organic phase obtained is washed with water, dried over magnesium sulfate and then evaporated under reduced pressure. 30 g of the expected product (yield: 80%) are obtained in the form of crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960758
Source datasetuspto-grants-1990_10
ORD IDord-c6caa68a70fd4db3b92c9fa4ade70935
Source noteuspto-grants-1990_10