참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,5-Dimethylaniline | HCID 7259 | — |
| 반응물 | Ethyl isobutyrylacetate | HCID 81583 | — |
| 생성물 | N-(2,5-dimethylphenyl)-4-methyl-3-oxopentanamide | HCID 86669288 | — |
반응 단계
A mixture of 2,5-dimethylaniline (7.70 g, 63.54 mmol) and ethyl 4-methyl-3-oxopentanoate (10.00 g, 1.0 eq) were refluxed at 160° C. overnight. After the reaction mixture was cooled to room temperature, it was triturated with hexane. The resulting precipitate was filtered and dried under high vacuum to yield the desired N-(2,5-dimethylphenyl)-4-methyl-3-oxopentanamide. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ ppm 1.18 (d, J=7.03 Hz, 6 H) 2.30 (d, J=7.62 Hz, 6 H) 2.66-2.85 (m, 1 H) 3.64 (s, 2 H) 6.87 (d, J=8.50 Hz, 1 H) 7.06 (d, J=7.62 Hz, 1 H) 7.77 (s, 1 H) 9.13 (br. s., 1 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08507682B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-b3ae5ecf57f947018f8a7e9a6734c8df |
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| 출처 메모 | uspto-grants-2013_08 |
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