돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52574생성일: 2026년 10월 25일

Pyridine → (But-3-enyloxy)(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/52574

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물3-Buten-1-olHCID 69389—
용매DichloromethaneHCID 6344—
생성물(But-3-enyloxy)(tert-butyl)dimethylsilaneHCID 1000806556.3%

반응 단계

Under a nitrogen atmosphere, to a cold (0° C.), stirring solution of 3-buten-1-ol (2.16 g, 30.0 mmol), pyridine (9 mL), and methylene chloride (30 mL) was added tert-butyldimethylsilyl chloride (4.53 g, 30.1 mmol) purchased from Aldrich Chemical Company. The ice-bath was removed and the mixture was allowed to stir 1 h at room temperature. The mixture, containing a white precipitate, was poured into water (60 mL) and shaken. The methylene chloride layer was separated from the aqueous layer, and the aqueous layer extracted with methylene chloride (30 mL). The two resulting organic extracts were combined, washed twice with water, dried (Na2SO4), filtered, and evaporated to give 8.94 g of crude product. Vacuum distillation afforded several fractions, the fraction with bp 80°-82° C. at 35 mm Hg was collected to give 3.14 g (56.3%) of product as an oil. 1H NMR (CDCl3): δ 5.86-5.73 (m, 1H), 5.08-4.98 (m, 2H), 3.64 (t, 2H), 2.29-2.22 (m, 2H), 0.87 (s, 9H), 0.03 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616716
출처 데이터셋uspto-grants-1997_04
ORD IDord-6f9457837d5743a1bb20f524255e0578
출처 메모uspto-grants-1997_04