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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18399생성일: 2026년 10월 23일

Imidazole → 3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile

https://huagongshe.com/ko/reaction/18399

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DimethylformamideHCID 6228—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물3-Hydroxy-3-(pyridin-4-yl)propanenitrileHCID 21973939—
용매Diethyl EtherHCID 3283—
용매Ethyl AcetateHCID 8857—
생성물3-(t-Butyldiphenylsiloxy)-3-(4-pyridyl)propionitrileHCID 2197421998.9%

반응 단계

Next, imidazole (4.60 g, 67.5 mmol) and N,N-dimethylformamide (30 ml) were added to the obtained 3-hydroxy-3-(4-pyridyl)propionitrile (1.00 g, 6.75 mmol), and the mixture was stirred at room temperature. t-Butyldiphenylchlorosilane (2.23 g, 8.10 mmol) was added to the mixture, and the whole was stirred for one day and then stirred further at an external temperature of 50° C. for three hours. Ethyl acetate (50 ml) and ether (50 ml) were added thereto, and the whole was washed with water (20 ml) three times and saturated brine (30 ml) successively. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 3-(t-butyldiphenylsiloxy)-3-(4-pyridyl)propionitrile (2.58 g, 98.9%) as a colorless oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741346B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1afb9fe9375140518b7d7d258c08a4b4
출처 메모uspto-grants-2010_06