돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1886757생성일: 2026년 10월 26일

Ethyl Acetate → 3-Methoxy-3-methylbutyl 2-(trifluoromethyl)benzenesulfonate

https://huagongshe.com/reaction/1886757

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물MethoxymethylbutanolHCID 62118—
반응물2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
반응물Sodium BicarbonateHCID 516892—
용매DichloromethaneHCID 6344—
생성물3-Methoxy-3-methylbutyl 2-(trifluoromethyl)benzenesulfonateHCID 8676198081%

반응 단계

To a solution of 3-methoxy-3-methylbutane-1-ol (2.8 g, 24 mmol) and TEA (1.6 g, 16 mmol) in CH2Cl2 (15 mL) was added o-(trifluoromethyl)benzenesulfonyl chloride (1.9 g, 8 mmol) dissolved in CH2Cl2 (20 mL). The solution was stirred at rt for 4 h. Saturated aqueous NaHCO3 (15 mL) was added to the solution and 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 8.23 (m, 1H), 7.91 (m, 1H), 7.74 (m, 2H), 4.25 (t, 2H, J=7.5 Hz), 3.10 (s, 1H), 1.92 (t, 2H, J=7.5 Hz) 1.13 (s, 6H). Anal. Calcd. For C13H17F3O4S: C, 47.85; H, 5.25. Found: C, 47.95; H, 5.11.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501382B1
출처 데이터셋uspto-grants-2013_08
ORD IDord-51a9dd8ec2754270a4e744d4f2d4bb49
출처 메모uspto-grants-2013_08