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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091179Generated: October 31, 2026

Nitromethane → 2-Ethyl-1-(5-methoxy-3-methyl-1-benzofuran-2-yl)butan-1-one

https://huagongshe.com/reaction/2091179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
Reactant2-Ethylbutyryl chlorideHCID 75954—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Methoxy-3-methylbenzofuranHCID 13156998—
SolventWaterHCID 962—
Product2-Ethyl-1-(5-methoxy-3-methyl-1-benzofuran-2-yl)butan-1-oneHCID 6677813897%

Reaction Steps

To a mixture of 5-methoxy-3-methyl-1-benzofuran (2.00 g) synthesized above, 2-ethylbutanoyl chloride (1.85 mL) and nitromethane (30 mL) was added aluminum chloride (3.28 g), and the mixture was stirred at room temperature for 1.5 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 (6% ethyl acetate/hexane) to give the title object compound (3.12 g, 97%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-4f07b6612afe40f8963917f8129a0926
Source noteuspto-grants-2013_05