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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15351생성일: 2026년 10월 26일

Water → 7-({[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}methyl)-2,3-dihydro-5(1H)-indolizinone

https://huagongshe.com/reaction/15351

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물3-[4-({[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}methyl)-6-(methyloxy)-2-pyridinyl]-1-propanolHCID 57486891—
촉매Tetrabutylammonium IodideHCID 67553—
용매DichloromethaneHCID 6344—
생성물7-({[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}methyl)-2,3-dihydro-5(1H)-indolizinoneHCID 5748689284.9%

반응 단계

A solution of 3-[4-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-6-(methyloxy)-2-pyridinyl]-1-propanol (5.16 g, 16.59 mmol) in dichloromethane (250 ml) was treated with pyridine (2.94 ml, 36.47 mmol) and trifluoromethanesulfonic anhydride (3.1 ml, 19.88 mmol) and stirred at room temperature for 10 min before being treated with tetrabutylammonium iodide (30.61 g, 82.95 mmol) and stirred at room temperature for a further 4 h. Water was then added and the mixture was extracted three times with diethyl ether and the combined organic extracts washed again with water. The organic extracts were dried with magnesium sulphate and evaporated. The residue was chromatographed on silica eluting with 0-10% methanol in dichloromethane to give the desired product (3.93 g, 14.09 mmol)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732461B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3cf1578bc419485980131438e0738c79
출처 메모uspto-grants-2010_06