関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine N-Oxide | HCID 12753 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | Ammonium Carbonate | HCID 517111 | — |
| 反応物 | Methyl 5-bromo-3,3-dimethylpentanoate | HCID 15276782 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Methyl 3,3-dimethyl-5-oxovalerate | HCID 3018723 | 63% |
反応手順
A mixture of methyl 5-bromo-3,3-dimethylpentanoate (5.0 g), pyridine-N-oxide (4.49 g), sodium bicarbonate (3.77 g) and toluene (30 cm3) was heated at the reflux temperature with vigorous agitation for a period of 14 hours. After cooling the mixture to the ambient temperature, water (20 cm3), saturated ammonium carbonate solution (20 cm3) and toluene (50 cm3) were added and the aqueous phase separated and extracted with toluene (3×75 cm3). The toluene extracts were added to the main organic phase and the whole dried over anhydrous magnesium sulphate concentrated by evaporation of the more volatile components under reduced pressure. The residual liquid was purified by Kugelrohr distillation (130° C./water pump pressure) to give methyl 3,3-dimethyl-5-oxopentanoate in 63% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05756835 |
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| 出典データセット | uspto-grants-1998_05 |
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| ORD ID | ord-b85c1265d2ff41958485e1e241bb73ee |
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| 出典メモ | uspto-grants-1998_05 |
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