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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390606생성일: 2026년 10월 26일

Sodium hydride → Ethyl 2-[1-(3'-methylaminobiphenyl-4-yl)meth-(e)-ylidene]butyrate

https://huagongshe.com/reaction/390606

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 2-(diethoxyphosphoryl)butanoateHCID 229053—
반응물3'-Methylaminobiphenyl-4-carbaldehydeHCID 1394524—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-[1-(3'-methylaminobiphenyl-4-yl)meth-(e)-ylidene]butyrateHCID 6896249672%

반응 단계

197 mg (4.9 mmol) of sodium hydride are added to a mixture of 1.2 mL (4.9 mmol) of triethyl 2-phosphonobutyrate and 415 mg of 3′-methylaminobiphenyl-4-carbaldehyde (2.0 mmol) in 10 mL of tetrahydrofuran. The reaction mixture is stirred at room temperature overnight, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over sodium sulfate. The solvent is evaporated off and the residue (1.1 g) is purified by chromatography on a column of silica eluted with a 90/10 heptane/ethyl acetate mixture. 438 mg (72%) of ethyl 2-[1-(3′-methylaminobiphenyl-4-yl)meth-(E)-ylidene]butyrate are obtained in the form of off-white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383652B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-919b2e7b34d54fd6b60e8686154cb1ac
출처 메모uspto-grants-2013_02