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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929748Generated: November 3, 2026

Hydrochloric Acid → HCID 86628629, compound

https://huagongshe.com/reaction/1929748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant2-Chlorobenzyl chlorideHCID 11906—
Reactant4-ChlorobenzonitrileHCID 12163—
ReactantMagnesiumHCID 5462224—
ReactantEther tetrahydrofuranHCID 21868444—
SolventDiethyl EtherHCID 3283—
ProductHCID 86628629HCID 8662862974%

Reaction Steps

To diethylether (250 mL) was added magnesium (6.04 g) and a catalytic amount of iodine and the mixture was stirred and thereto was gradually added dropwise 2-chlorobenzyl chloride (20.0 g). After stirring for 1 hour from the time when the temperature of such mixture began to rise, thereto was added a solution of 4-chlorobenzonitrile (18.8 g) in tetrahydrofuran/diethylether (20 mL/50 mL) and the mixture was stirred for 3 hours. To the reaction mixture was added 2N HCl (150 mL) under ice-cooling and the mixture was stirred at room temperature for 2 hours. The reaction mixture was extracted with ethyl acetate and the organic layer was washed with 1N HCl, water and saturated brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=40/1 to 20/1) to obtain 2-(chlorobenzyl)(4-chlorophenyl)methanone (24.40 g; yield: 74%) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188097B2
Source datasetuspto-grants-2012_05
ORD IDord-b87bdc0e8e584f1db8d78064c1cd1eb6
Source noteuspto-grants-2012_05