関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | tert-Butanol | HCID 6386 | — |
| 反応物 | 2-Bromo-1-thiophen-3-yl-butan-1-one | HCID 59598618 | — |
| 反応物 | HCID 178461630 | HCID 178461630 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 2-Bromo-1-thiophen-3-yl-butan-1-one | HCID 59598618 | — |
| 生成物 | 5-Thiophen-3-yl-heptane-2,4-dione | HCID 59598638 | — |
反応手順
EtMgBr (6.69 ml, 13 mmol, 2 M in ethyl ether) in benzene (10 ml) was cooled to zero degrees C., and tBuOH (1.28 ml, 13 mmol) was slowly added. The reaction mixture was stirred at zero degrees C. for 5 minutes, then acetone (530 ul, 7 mmol) was added, followed by a solution of 2-Bromo-1-thiophen-3-yl-butan-1-one (1.3 g, 6 mmol) in 3 ml benzene via cannula. The reaction mixture was heated to reflux for 1 hour, and acetone (250 ul) was added. The reaction mixture was heated 2 hours more at reflux. The reaction was cooled, quenched with 1 N HCl (10 ml), extracted three times with diethyl ether, washed brine, and dried over magnesium sulfate. The solvent was removed in vacuo and the residue chromatographed (5% ethyl acetate/hexanes) to give 247 mg of 2-Bromo-1-thiophen-3-yl-butan-1-one starting material and 520 mg of 5-Thiophen-3-yl-heptane-2,4-dione, 44%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846705B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-33848afc06574e7288b8338ac9572e89 |
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| 出典メモ | uspto-grants-2014_09 |
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