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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091403Generated: November 1, 2026

Water → 1-(5-Fluoro-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-one

https://huagongshe.com/reaction/2091403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutyryl chlorideHCID 62325—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Fluoro-3-methylbenzofuranHCID 11679847—
SolventNitromethaneHCID 6375—
Product1-(5-Fluoro-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-oneHCID 6677784866%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-fluoro-3-methyl-1-benzofuran (2.0 g) synthesized in Example A67(2) and isobutyryl chloride (1.56 g) in nitromethane (40 mL) was added aluminum chloride (anhydrous) (2.66 g) at 0° C., and the mixture was stirred at 0° C. for 1 hr, and at room temperature for 12 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated. The residue was subjected to silica gel column chromatography (hexane-ethyl acetate 100:0-90:10, v/v) to give the title compound (1.933 g, 66%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-51515ff4f24240d8bf5b68f24de5550f
Source noteuspto-grants-2013_05