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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171657생성일: 2026년 10월 27일

Ammonium Chloride → (E)-3-[(Pyrrol-2-yl)methylidene]-1-(triphenylmethyl)piperidin-4-one

https://huagongshe.com/reaction/1171657

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-Tritylpiperidin-4-oneHCID 2748414—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물tert-Butyl 2-formyl-1H-pyrrole-1-carboxylateHCID 5057005—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-[(Pyrrol-2-yl)methylidene]-1-(triphenylmethyl)piperidin-4-oneHCID 2313876935%

반응 단계

To a solution of 1-(triphenylmethyl)piperidin-4-one (17.00 g) in tetrahydrofuran (400 ml) was added dropwise a 0.5N solution of potassium bis(trimethylsilyl)amide in toluene (100 ml) at −70° C., and the resulting mixture was stirred at the same temperature for 20 minutes. Subsequently, to the reaction mixture was added dropwise a solution of 1-(t-butoxycarbonyl)pyrrole-2-carbaldehyde (11.00 g) in tetrahydrofuran (100 ml) at −70° C., and the resulting mixture was stirred at the same temperature for 1 hour. After saturated aqueous ammonium chloride solution was added, the resulting reaction mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution and the organic layer was dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate, hexane, and dichloromethane (1:3:1) as the eluent to afford the title compound (7.26 g, yield: 35%) as a yellow amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829580B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-c8197e42b60344b9ba78b7da8b756cb7
출처 메모uspto-grants-2010_11