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HRID 14316生成日期:2026年10月23日

丙酮 → 4-[(Methylsulfonyl)methyl]cyclohexanecarboxylic acid

https://huagongshe.com/zh-CN/reaction/14316

反应方程式

参与物

角色名称HCID投料
反应物丙酮HCID 180—
反应物碳酸氢钠HCID 516892—
反应物4-[(Methylthio)methyl]cyclohexanecarboxylic acidHCID 21085950—
反应物Potassium hydroxy sulfiteHCID 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 acidHCID 2108594990.8%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07727997B2
来源数据集uspto-grants-2010_06
ORD IDord-618f895760604f8f97d25ee748018ef9
来源说明uspto-grants-2010_06