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Acetone → 4-Hydroxy-4-methylcyclohexanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| 反応物 | 8-Methyl-1,4-dioxaspiro(4.5)decan-8-ol | HCID 18713075 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-Hydroxy-4-methylcyclohexanone | HCID 28539 | 86% |
反応手順
To a solution of 8-methyl-1,4-dioxaspiro[4.5]decan-8-ol (1 equiv) in a 2:1 mixture of acetone and water (0.38 M) was added pyridinium p-toluenesulfonate (0.2 equiv).The resulting mixture was refluxed for 8 h. After the reaction was complete, the reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel chromatography (0-30% ethyl acetate in petroleum ether) to afford the title compound (86% yield) as a yellow solid. 1H NMR (400 MHz, CHLOROFORM-d1) δ ppm 3.96-3.93 (m, 2H), 2.27-2.25 (m, 1H), 2.25-2.22 (m, 1H), 2.01-1.94 (m, 2H), 1.90-1.82 (m, 2H), 1.38 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09346812B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-210ffaa0bdbb462bb98f4ccc653c7b83 |
| 出典メモ | uspto-grants-2016_05 |