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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479602생성일: 2026년 10월 27일

Tetrahydrofuran → Ethyl 4-(4-benzyloxyphenyl)-2-cyano-3-phenylbutyrate

https://huagongshe.com/reaction/479602

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물4-Benzyloxybenzyl chlorideHCID 70042—
반응물Ethyl benzylidenecyanoacetateHCID 74845—
용매TolueneHCID 1140—
생성물Ethyl 4-(4-benzyloxyphenyl)-2-cyano-3-phenylbutyrateHCID 18772157—

반응 단계

835 mg of Mg are suspended in 5 ml of abs. THF. A solution of 2.0 g of 4-benzyloxybenzyl chloride in 5 ml of abs. tetrahydrofuran is subsequently added dropwise. When the addition is complete, the cloudy solution is stirred at room temperature for a further 1 hour, a solution of 1.73 g of ethyl 2-cyano-3-phenylacrylate in 10 ml of abs. toluene is subsequently added, and the mixture is refluxed for 16 hours. The solvent is removed, and conventional work-up gives ethyl 4-(4-benzyloxyphenyl)-2-cyano-3-phenylbutyrate (“AA”).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06645991B1
출처 데이터셋uspto-grants-2003_11
ORD IDord-63baf29a43f746389e4276ede39451d5
출처 메모uspto-grants-2003_11