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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Fluoro-3-methylbenzofuran | HCID 11679847 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 1-(5-Fluoro-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-one | HCID 66777848 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436043B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-51515ff4f24240d8bf5b68f24de5550f |
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| Source note | uspto-grants-2013_05 |
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