돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 481715생성일: 2026년 10월 26일

Imidazole → 1-t-BUTYLDIMETHYLSILYLOXY-2,3-DIMERCAPTOPROPANE

https://huagongshe.com/reaction/481715

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DimercaprolHCID 3080—
반응물Ammonium ChlorideHCID 25517—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
용매TetrahydrofuranHCID 8028—
생성물1-t-BUTYLDIMETHYLSILYLOXY-2,3-DIMERCAPTOPROPANEHCID 2125583994.6%

반응 조건

온도0 °C

반응 단계

To a solution of 2,3-dimercapto-1-propanol (15.0 ml, 150 mmol) and imidazole (15.3 g, 224 mmol, 1.5 eq) in THF (300 mL) was added t-butyldimethylsilyl chloride (21.4 g, 142 mmol, 0.95 eq) at 0° C. The mixture was stirred at 0° C. for 1 hr and at room temperature for 18 hr. A saturated solution of ammonium chloride was added and the aqueous phase was extracted with dichloromethane. The organic layer was dried with anhydrous sodium sulphate and the solvent was evaporated under reduced pressure. The crude material was purified by flash chromatography with a mixture of hexane and ethyl acetate (90:10) to give the pure compound (32.04 g) in 94.5% yield. 1H NMR (300 MHz, CDCl3) δ: 0.08 (s, 6H, CH3), 0.91 (s, 9H, t-butyl), 1.58 (t, 1H, J=8.5 Hz, SH), 1.82 (d, 1H, J=9.2 Hz, SH), 2.85 (m, 2H, H-3), 2.96 (m, 1H, H-2), 3.63 (dd, 1H, J=6.7 Hz, 10.1 Hz, H-1a), 3.86 (dd, 1H, J=4.4 Hz, 10.2 Hz, H-1b).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05789394
출처 데이터셋uspto-grants-1998_08
ORD IDord-ad76ac018c194b9b898e6e71883e7e96
출처 메모uspto-grants-1998_08