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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708553Generated: October 30, 2026

1-(4-((3,4-Dichlorobenzyl)oxy)phenyl)ethanone → 2-Bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanone

https://huagongshe.com/reaction/708553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-((3,4-Dichlorobenzyl)oxy)phenyl)ethanoneHCID 2775031—
SolventDichloromethane methanolHCID 21226129—
Product2-Bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanoneHCID 58327574—

Reaction Steps

1-[4-(3,4-Dichloro-benzyloxy)-phenyl]-ethanone (2.92 g) was dissolved in methanol:DCM (2:1, 75 mL) and pyrolidinone hydrotribromide (7.5 g) was added and stirred at room temperature for 2.5 h. After completion of the reaction, the mixture was concentrated in vacuo and poured into saturated sodium bicarbonate solution (100 mL) and extracted with ethyl acetate (2×100 mL). The organic extracts were combined and concentrated in vacuo. Then this residue was dissolved in DCM (10 ml) and methanol (10 mL) was slowly added to this solution to precipitate the product. The colored solution was filtered through to give clear white powder product 2-bromo-1-[4-(3,4-dichloro-benzyloxy)-phenyl]-ethanone with quantitative yield (3.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175003B2
Source datasetuspto-grants-2015_11
ORD IDord-8e98e01822dc46d1a2cc0425fb5146ec
Source noteuspto-grants-2015_11