돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1886758생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1886758

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물MethoxymethylbutanolHCID 62118—
반응물2,3,4,5,6-Pentafluorobenzenesulfonyl chlorideHCID 70026—
반응물Sodium BicarbonateHCID 516892—
용매DichloromethaneHCID 6344—
생성물3-Methoxy-3-methylbutyl 2,3,4,5,6-pentafluorobenzenesulfonateHCID 86761981163%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501382B1
출처 데이터셋uspto-grants-2013_08
ORD IDord-fbcc8750462240ca90d2ca47cbe9584a
출처 메모uspto-grants-2013_08