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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107863Generated: October 30, 2026

Carbon Dioxide → 7-BROMO-2,3-DIMETHYL-1-BENZOFURAN

https://huagongshe.com/reaction/1107863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 15381110HCID 15381110—
SolventAcetoneHCID 180—
Product7-BROMO-2,3-DIMETHYL-1-BENZOFURANHCID 1109626291.4%

Reaction Steps

25 ml of concentrated sulphuric acid are introduced into a 100 ml three-necked flask equipped with a thermometer and a 10 ml dropping funnel and cooling is carried out to between -15 and 0° C. with a bath of solid carbon dioxide in acetone. 3-(2-Bromophenoxy)-2-butanone (5 g, 20.6 mmol) is added dropwise and stirring is continued for 5 min. The mixture is poured onto crushed ice and then extraction is carried out with ethyl acetate (3×80 ml). The organic phases are combined, dried over magnesium sulphate and concentrated. The residue is purified by silica column chromatography (elution solvent: cyclohexane). 4.24 g (Yield: 91%) of 2,3-dimethyl-7-bromobenzofuran are obtained--M.p.: 33° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063810
Source datasetuspto-grants-2000_05
ORD IDord-3967f8d9b6504b879c696d25a1cd0ce8
Source noteuspto-grants-2000_05