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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598890Generated: October 31, 2026

Hydrochloric Acid → 4-Bromo-2-(cyanomethyl)benzonitrile

https://huagongshe.com/reaction/598890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl cyanoacetateHCID 7747—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-Bromo-2-(cyanomethyl)benzonitrileHCID 1604991678.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (47.2 g, 1.18 mol) was suspended in 320 mL DMSO and cooled to 0° C. in an ice-water bath. The mixture became viscous as the DMSO began to freeze. Methyl cyanoacetate (104 mL, 1.18 mol) was added slowly causing a slight temperature increase and thus a more easily stirrable solution. The mixture was stirred for 30 minutes at room temperature. 4-Bromo-2-fluorobenzonitrile (118 g, 590 mmol) (commercially available from Acros Organics (Order Number 29049)) was added via cannula as a solution in 500 mL DMSO. The mixture was heated to an internal temperature of 90° C. The mixture was cooled and allowed to stand overnight. 1.2 L of water was added to the reaction mixture. The mixture was heated to an internal temperature of 104° C. over 3 hours. 2.3 L of water was added and the mixture was heated at reflux 16 hours. The mixture was cooled to 5° C. and 700 mL of 0.2N HCl was added. The mixture was allowed to stir at 5° C. for 30 minutes. The resulting precipitate was filtered, washed with water, and dried to provide the product (102 g, 78%). LCMS (API-ES) m/z: 223, 221 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-42716c64b5264e69835490d9e21ac5c6
Source noteuspto-grants-2011_03