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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237069Generated: October 27, 2026

Dibenzofuran → Dibenzofuran-2-ylethan-2-one

https://huagongshe.com/reaction/2237069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzofuranHCID 568—
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductDibenzofuran-2-ylethan-2-oneHCID 13477039—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of dibenzofuran (0.5 mmol) in anhydrous DCM was cooled to 0° C. AlCl3 (1.5 eq., 0.75 mmol) was added followed by a slow addition of acetyl chloride (1.5 eq., 0.75 mmol). The reaction mixture was stirred at 0° C. for 2-3 h or until the completion of reaction. The product was extracted with DCM and washed with saturated sodium bicarbonate solution. The organic layer was dried over anhydrous sodium sulfate and concenterated in vacuo to give dibenzofuran-2-ylethan-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714013B2
Source datasetuspto-grants-2010_05
ORD IDord-ebae6c74b685496fa13ea55f2554cd97
Source noteuspto-grants-2010_05