Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409539Generated: October 30, 2026

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

https://huagongshe.com/reaction/1409539

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 numberUS08921380B2
Source datasetuspto-grants-2014_12
ORD IDord-477b9cd8fb05468595b952aab2f86e16
Source noteuspto-grants-2014_12