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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762224Generated: November 1, 2026

Benzonitrile → HCID 13431722, compound

https://huagongshe.com/reaction/1762224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantSodium HydroxideHCID 14798—
ReactantSilicon tetrachlorideHCID 24816—
Reactant1-Methyl-N-phenylpiperidin-4-amineHCID 89642—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 13431722HCID 1343172271%

Reaction Steps

To a solution of 0.38 g (2 mmol) of 4-anilino-1-methyl-piperidine 1 dissolved in 10 ml of 1.2-dichloroethane are added 0.3 ml (2×1.2 mmol) of boron trifluoride ether adduct, 0.28 ml (2×1.2 mmol) of silicon tetrachloride, and 0.41 ml (2×2 mmol) of benzonitrile at room temperature with stirring, and the mixture is heated under reflux with stirring for 20 hours. The reaction mixture is cooled and a solution of 2.5 g of sodium hydroxide dissolved in 10 ml of water and 4 ml of methanol are added thereto with stirring under ice-cooling. The mixture is stirred at room temperature for 1 hour and extracted with dichloromethane; the organic layer is washed with water, dried over anhydrous magnesium sulfate, and concentrated. The resulting residue is recrystallized from ether-petroleum ether to give 414 mg of crystalline 2-(1-methyl-4-piperidinyl)aminobenzophenone imine 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831132
Source datasetuspto-grants-1989_05
ORD IDord-faddd23ce8cd4d2aa7b4846a55b568b8
Source noteuspto-grants-1989_05