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HRID 390630생성일: 2026년 10월 25일

Sodium hydride → Ethyl 2-[1-(3-butoxy-4-iodophenyl)meth-(e)-ylidene]butyrate

https://huagongshe.com/reaction/390630

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 2-(diethoxyphosphoryl)butanoateHCID 229053—
반응물3-Butoxy-4-iodobenzaldehydeHCID 59574930—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-[1-(3-butoxy-4-iodophenyl)meth-(e)-ylidene]butyrateHCID 6895709397%

반응 단계

A solution of 9 mL (37.8 mmol) of triethyl 2-phosphonobutyrate in 20 mL of tetrahydrofuran is added to a mixture of 1.52 g (37.8 mmol) of sodium hydride in 15 mL of tetrahydrofuran. The reaction medium is stirred for 20 minutes. A solution of 3.83 g (12.6 mmol) of 3-butoxy-4-iodobenzaldehyde (prepared as described in Example 19g) in 15 mL of tetrahydrofuran is then added to the reaction mixture and the reaction medium is stirred at room temperature for 2 hours 30 minutes. The reaction medium is poured into saturated ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated off and the residue (11.49 g) is purified by chromatography on silica gel eluted with a 95/5 heptane/ethyl acetate mixture. 4.90 g (97%) of ethyl 2-[1-(3-butoxy-4-iodophenyl)meth-(E)-ylidene]butyrate are obtained in the form of a yellow oil that crystallizes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383652B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-6012fff6f90741bea1e705721ba92685
출처 메모uspto-grants-2013_02