HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349105Erstellt: 26. Oktober 2026
Acetone → 4-[(Methylsulfonyl)methyl]cyclohexanecarboxylic acid
https://huagongshe.com/reaction/349105
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4-[(Methylthio)methyl]cyclohexanecarboxylic acid | HCID 21085950 | — |
| Edukt | Potassium hydroxy sulfite | HCID 23707502 | — |
| Lösungsmittel | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Lösungsmittel | Sodium Hydroxide | HCID 14798 | — |
| Produkt | 4-[(Methylsulfonyl)methyl]cyclohexanecarboxylic acid | HCID 21085949 | 90,8% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07176242B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-632c93e23dff4b7cb504f7b477bedfe2 |
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| Quellennotiz | uspto-grants-2007_02 |
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