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HRID 1886758Erstellt: 25. Oktober 2026

Ethyl Acetate → 3-Methoxy-3-methylbutyl 2,3,4,5,6-pentafluorobenzenesulfonate

https://huagongshe.com/reaction/1886758

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktMethoxymethylbutanolHCID 62118—
Edukt2,3,4,5,6-Pentafluorobenzenesulfonyl chlorideHCID 70026—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Methoxy-3-methylbutyl 2,3,4,5,6-pentafluorobenzenesulfonateHCID 86761981163%

Reaktionsschritte

To a solution of 3-methoxy-3-methylbutane-1-ol (1.07 g, 9 mmol) and TEA (0.61 g, 6 mmol) in CH2Cl2 (12 mL) was added pentafluorobenzenesulfonyl chloride (0.99 g, 3.7 mmol). The solution was stirred at rt for 2 h. Saturated aqueous NaHCO3 (12 mL) was added to the solution and the mixture was stirred at rt for 30 min. The organics were extracted with CH2Cl2 (75 mL) and washed with 1 M HCl (2×25 mL), saturated aqueous NaHCO3 (1×25 mL) and saturated aqueous NaCl (1×25 mL). The organics were dried over Na2SO4 and concentrated to give a crude mixture. Silica gel chromatography with ethyl acetate in hexanes yielded the desired product (2.1 g, 81%). 1H NMR (400 MHz CDCl3) δ 4.42 (t, 2H, J=7.3 Hz), 3.13 (s, 3H), 1.97 (t, 2H, J=7.4 Hz), 1.17 (s, 6H); 19F NMR (400 MHz CDCl3) δ −137.9 (m, 2H), −146.65 (m, 1H), −161.01 (m, 2H). Anal. Calcd. For C12H13F5O4S: C, 41.38; H, 3.76. Found: C, 41.37; H, 3.77.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08501382B1
Quelldatensatzuspto-grants-2013_08
ORD IDord-fbcc8750462240ca90d2ca47cbe9584a
Quellennotizuspto-grants-2013_08