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HRID 2247633생성일: 2026년 10월 23일

Dimethylformamide → 5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-3-furaldehyde

https://huagongshe.com/ko/reaction/2247633

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ammonium ChlorideHCID 25517—
반응물[(4-Bromo-2-furyl)methoxy](t-butyl)dimethylsilaneHCID 68521066—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-3-furaldehydeHCID 8662020955%

반응 단계

To a solution of [(4-bromo-2-furyl)methoxy](t-butyl)dimethylsilane (7.3 g, 25 mmol) that was obtained in Example 1 (1a) in tetrahydrofuran (50 ml) was slowly added dropwise n-butyllithium (a 1.6 M solution in hexane, 17 ml, 28 mmol) at −78° C. with stirring, and the resulting mixture was stirred for 5 minutes. Subsequently, to the reaction mixture was furthermore added N,N-dimethylformamide (3.8 ml, 50 mmol) at the same temperature with stirring, and the resulting mixture was stirred for 45 minutes. After stirring, a saturated aqueous solution of ammonium chloride (10 ml) was added to the reaction mixture to quench the reaction, and the resulting mixture was poured into water (100 ml) and extracted with ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:49 to 1:19) as the eluent to afford the title compound (3.3 g) in a yield of 55% as a colourless oily product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07687491B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-f4990ec302e04b3b8851a47d68195e7f
출처 메모uspto-grants-2010_03