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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696182Generated: November 1, 2026

1,2-Dimethoxyethane → (2-chlorobenzyl)(4-chlorophenyl)methanone

https://huagongshe.com/reaction/1696182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
CatalystZincHCID 23994—
CatalystHCID 178418476HCID 178418476—
Product(2-chlorobenzyl)(4-chlorophenyl)methanoneHCID 24659991%

Reaction Steps

To dimethoxyethane (100 mL) were added 4-chlorobenzyl bromide (4.1 g), 4-chlorobenzoyl chloride (2.56 mL), bis(triphenylphosphine)palladium dichloride (702 mg) and zinc powder (2.6 g), and the mixture was stirred for 2 hours under nitrogen atmosphere. The reaction mixture was filtered and the filtrate was concentrated in vacuo and extracted with ethyl acetate. The organic layer was washed with 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=49/1 to 9/1) to give (2-chlorobenzyl)(4-chlorophenyl)-methanone (4.85 g, yield: 91%) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163759B2
Source datasetuspto-grants-2012_04
ORD IDord-8c5edf879f4e4fe89475ed7c46c5f623
Source noteuspto-grants-2012_04