HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → (5-Methoxy-3-methyl-1-benzofuran-2-yl)(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Methoxy-3-methylbenzofuran | HCID 13156998 | — |
| Solvent | Water | HCID 962 | — |
| Product | (5-Methoxy-3-methyl-1-benzofuran-2-yl)(phenyl)methanone | HCID 1473421 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-efc693a31d8e4f988e8f164f7f88f8c0 |
| Source note | uspto-grants-2013_05 |