参与物
| 角色 | 名称 | HCID | 投料 |
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| 反应物 | 丙酮 | HCID 180 | — |
| 反应物 | 碳酸氢钠 | HCID 516892 | — |
| 反应物 | 4-[(Methylthio)methyl]cyclohexanecarboxylic acid | HCID 21085950 | — |
| 反应物 | Potassium hydroxy sulfite | HCID 23707502 | — |
| 溶剂 | 乙二胺四乙酸二钠 | HCID 6049 | — |
| 溶剂 | 二甲基对苯二胺二盐酸 | HCID 14798 | — |
| 产物 | 4-[(Methylsulfonyl)methyl]cyclohexanecarboxylic acid | HCID 21085949 | 90.8% |
反应步骤
To a stirred solution of methyl sulfide from step 5 (100 mg, 0.5 mmol) in sodium hydroxide solution (1.5 mL, 0.5 M solution in water) was added sodium bicarbonate (360 mg, 4.3 mmol) and acetone (1 mL) followed by the addition of a solution of oxone (430 mg, 0.7 mmol) in 0.0004 M EDTA (2 mL). The reaction mixture was stirred at room temperature for 2 h and then quenched with sodium bisulfite. The reaction mixture was acidified with 1 N hydrochloric acid and extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with water, dried (sodium sulfate), filtered, and concentrated under reduced pressure to provide 4-[(methylsulfonyl)methyl]cyclohexanecarboxylic acid (100 mg): 1H NMR (300 MHz, CD3OD) δ 3.11-3.08 (m, 2H), 2.96 (s, 3H), 2.53-2.51 (m, 1H), 2.18-2.16 (m, 1H), 1.99-1.93 (m, 2H), 1.79-1.25 (m, 6H).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07727997B2 |
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| 来源数据集 | uspto-grants-2010_06 |
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| ORD ID | ord-618f895760604f8f97d25ee748018ef9 |
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| 来源说明 | uspto-grants-2010_06 |
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