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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1393161생성일: 2026년 10월 26일

Diethyl Ether → 2,2-Dimethyl-3-(pyridin-4-yl)propan-1-amine

https://huagongshe.com/reaction/1393161

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Sodium HydroxideHCID 14798—
반응물Aluminium lithium hydrideHCID 21226445—
반응물2,2-Dimethyl-3-(4-pyridyl)-3-(p-tolylsulfonyloxy)propionitrileHCID 21974022—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2,2-Dimethyl-3-(pyridin-4-yl)propan-1-amineHCID 1213664228%

반응 단계

Anhydrous diethyl ether (10 ml) was dropwise to lithium aluminum hydride (345 mg, 9.10 mmol) under a nitrogen atmosphere and ice-cold water-cooling. Then, a solution of 2,2-dimethyl-3-(4-pyridyl)-3-(p-tolylsulfonyloxy)propionitrile (600 mg, 1.82 mmol) in tetrahydrofuran (10 ml) was added dropwise to the mixture. The whole was stirred at room temperature overnight, and water (324 μl), a 15% aqueous sodium hydroxide solution (324 μl) and water (972 μl) were added successively to the reaction mixture while stirring it vigorously under ice-cold water-cooling. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the concentrate was purified by silica gel column chromatography to give the titled compound (83.0 mg, 0.505 mmol, 28%) as a pale yellow oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07345064B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-5854762690a14f08a0b2ece6c92b5f24
출처 메모uspto-grants-2008_03