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HRID 14316Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/14316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktSodium BicarbonateHCID 516892—
Edukt4-[(Methylthio)methyl]cyclohexanecarboxylic acidHCID 21085950—
EduktPotassium hydroxy sulfiteHCID 23707502—
LösungsmittelEthylenediaminetetraacetic AcidHCID 6049—
LösungsmittelSodium HydroxideHCID 14798—
Produkt4-[(Methylsulfonyl)methyl]cyclohexanecarboxylic acidHCID 2108594990,8%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-618f895760604f8f97d25ee748018ef9
Quellennotizuspto-grants-2010_06