関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | 3-Bromopyridine | HCID 12286 | — |
| 反応物 | Ethyl N-methoxy-N-methylcarbamate | HCID 533715 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 生成物 | Di-3-pyridinylmethanone | HCID 298471 | 33% |
反応手順
To a solution of 3-bromopyridine (9.84 g,0.062 mol) in 300 ml of ether cooled to -78° C. was added n-butyllithium (1.6M, 41 ml, 0.066 mol) and stirred for 30 min. N-Methyl,N-methoxy-urethane (3.76 g, 0.028 mol) in 20 ml of ether was added in 10 min, the mixture was stirred (-78° C.) for 1 h, allowed to warm to room temperature and stirred for 2 h. The reaction mixture was quenched with 6N HCl (100 ml) and stirred. The aqueous layer was basified with 10% NaOH solution, extracted with ethyl acetate (2×) and methylene dichloride. The organic layer was dried over sodium sulfate, concentrated in vacuo, and the residue was purified by chromatography on silica (ethyl acetate, 10% methanol/ethyl acetate) to afford 1,7 g (33%) of di-(3-pyridyl)ketone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05569655 |
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| 出典データセット | uspto-grants-1996_10 |
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| ORD ID | ord-56bdc5037f6e4079bd650a40e896aba8 |
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| 出典メモ | uspto-grants-1996_10 |
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