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HRID 1886758作成日:2026年10月27日

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

https://huagongshe.com/reaction/1886758

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物MethoxymethylbutanolHCID 62118—
反応物2,3,4,5,6-Pentafluorobenzenesulfonyl chlorideHCID 70026—
反応物Sodium BicarbonateHCID 516892—
溶媒DichloromethaneHCID 6344—
生成物3-Methoxy-3-methylbutyl 2,3,4,5,6-pentafluorobenzenesulfonateHCID 86761981163%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08501382B1
出典データセットuspto-grants-2013_08
ORD IDord-fbcc8750462240ca90d2ca47cbe9584a
出典メモuspto-grants-2013_08