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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1886760생성일: 2026년 10월 26일

1,3-Butanediol → 3-Hydroxybutyl 2,3,4,5,6-pentafluorobenzenesulfonate

https://huagongshe.com/reaction/1886760

반응식

참여 물질

역할이름HCID투입량
반응물1,3-ButanediolHCID 7896—
반응물Ethyl AcetateHCID 8857—
반응물2,3,4,5,6-Pentafluorobenzenesulfonyl chlorideHCID 70026—
반응물Sodium BicarbonateHCID 516892—
용매DichloromethaneHCID 6344—
생성물3-Hydroxybutyl 2,3,4,5,6-pentafluorobenzenesulfonateHCID 8676198340.6%

반응 단계

To a solution of 1,3-butane diol (0.9 g, 10 mmol) and TEA (0.61 g, 6 mmol) in CH2Cl2 (4 mL) at 0° C. was added pentafluorobenzenesulfonyl chloride (0.53 g, 2 mmol) dissolved in CH2Cl2 (4 mL). The solution was stirred for 6 h over which time the solution slowly warmed to rt. Saturated aqueous NaHCO3 (25 mL) was added to the solution and the mixture was stirred at rt for 30 min. The organics were extracted with CH2Cl2 (50 mL) and washed with 0.5 M HCl (3×20 mL), saturated aqueous NaHCO3 (1×20 mL) and saturated aqueous NaCl (1×20 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 (0.26 g, 40%). 1H NMR (400 MHz CDCl3) δ 4.62 (m, 2H), 4.13 (m, 1H), 2.11 (m, 1H), 1.94 (m, 1H), 1.40 (d, 3H, J=6.2 Hz). Anal. Calcd. For C10H9F5O4S: C, 37.51; H, 2.83. Found: C, 37.70; H, 2.93.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501382B1
출처 데이터셋uspto-grants-2013_08
ORD IDord-6bb7e369294d4c379d1e9ba61865503b
출처 메모uspto-grants-2013_08