참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzoyl chloride | HCID 7412 | — |
| 반응물 | 3,4-Dimethylanisole | HCID 78411 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Lithium perchlorate | HCID 23665649 | — |
| 촉매 | Scandium(III) triflate | HCID 2734571 | — |
| 용매 | Nitromethane | HCID 6375 | — |
| 생성물 | (2-Methoxy-4,5-dimethylphenyl)(phenyl)methanone | HCID 23078360 | 93% |
반응 단계
Commercially available 3,4-dimethylanisole (409 mg) was dissolved in nitromethane (6 ml) to prepare a solution. Lithium perchlorate (1.9 g) and benzoyl chloride (843 mg) were added to the solution, scandium trifluoromethanesulfonate (148 mg) was then added thereto, and the mixture was stirred at room temperature for 3 days. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate and was concentrated. The residue was subjected to separation and purification by column chromatography on silica gel using hexane/ethyl acetate as a solvent to give (4,5-dimethyl-2-methoxyphenyl)(phenyl)methanone (667 mg, yield 93%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07560558B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-802b722db74e4c3998754ed0872a693d |
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| 출처 메모 | uspto-grants-2009_07 |
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