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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091212Generated: November 3, 2026

Nitromethane → (5-Methoxy-3-methyl-1-benzofuran-2-yl)(phenyl)methanone

https://huagongshe.com/reaction/2091212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantBenzoyl chlorideHCID 7412—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Methoxy-3-methylbenzofuranHCID 13156998—
SolventWaterHCID 962—
Product(5-Methoxy-3-methyl-1-benzofuran-2-yl)(phenyl)methanoneHCID 147342162%

Reaction Steps

To a mixture of 5-methoxy-3-methyl-1-benzofuran (2.00 g) synthesized in Example A104(2), benzoyl chloride (1.68 mL) and nitromethane (20 mL) was added aluminum chloride (3.28 g), and the mixture was stirred at room temperature for 2 hr. Water was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30% ethyl acetate/hexane) and further by silica gel column chromatography (20% ethyl acetate/hexane) to give the title object compound (2.03 g, 62%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-efc693a31d8e4f988e8f164f7f88f8c0
Source noteuspto-grants-2013_05