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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882772Generated: November 1, 2026

Aniline → HCID 23509657, compound

https://huagongshe.com/reaction/1882772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantSodium hydrideHCID 24758—
Reactant2-Cyano-3-fluorobiphenylHCID 23509652—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 23509657HCID 23509657—

Reaction Steps

Aniline (0.168 g, 1.8 mmol) was dissolved in dimethyl sulfoxide (3 mL) and stirred under argon at room temperature. Sodium hydride (0.0043 g, 1.8 mmol) was added and a deep purple color developed while the mixture was stirred at room temperature for 1 hour. The mixture was cooled to 0° C. in an ice bath and the product of example 12a above, 2-fluoro-6-phenylbenzonitrile, (0.295 g, 1.5 mmol) dissolved in dimethyl sulfoxide (2 mL) was added and the mixture stirred at room temperature overnight. The solvent was evaporated in vacuo, and the residue was partitioned between ethyl acetate and water. The organic phase was washed with water (5×), brine (1×) dried over anhydrous Na2SO4 filtered, and evaporated to give the crude product which was then chromatographed on silica gel eluted with 0-30% CH2Cl2 in hexane to give the title compound as a white amorphous solid. ES (+) MS m/e=271 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759410B1
Source datasetuspto-grants-2004_07
ORD IDord-96840d836ee046a4b100dd1951904438
Source noteuspto-grants-2004_07