참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N-Dimethylaniline | HCID 949 | — |
| 반응물 | Butyryl chloride | HCID 8855 | — |
| 반응물 | 2-Amino-4-methyl-3-nitropyridine | HCID 243166 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-Butyrylamino-4-methyl-3-nitropyridine | HCID 21464239 | — |
반응 단계
A mixture of 2-amino-4-methyl-3nitropyridine (5.0 g) and N,N-dimethylaniline (8.5 ml) was heated at 100° C. under nitrogen atmosphere. To the solution was added butyryl chloride (3.5 ml) and the mixture was stirred at 100° C. for 5 hours. After being cooled to room temperature, ethyl acetate was added to the reaction mixture. The organic layer was separated and washed successively with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo. The residue was washed with n-hexane to give 2-butyrylamino-4-methyl-3-nitropyridine (7.0 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05210092 |
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| 출처 데이터셋 | uspto-grants-1993_05 |
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| ORD ID | ord-9777e84daa0943d1869c526e16dd47ee |
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| 출처 메모 | uspto-grants-1993_05 |
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