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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 361893생성일: 2026년 10월 26일

Citric Acid → ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(5-cyano-2-benzofuranyl)acrylate

https://huagongshe.com/reaction/361893

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물(5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chlorideHCID 21844326—
반응물ethyl 2-[4-[((3S)-1-tert-butoxy-carbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetateHCID 86753663—
용매EthanolHCID 702—
용매Toluene ethylacetateHCID 21584019—
생성물ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(5-cyano-2-benzofuranyl)acrylateHCID 57233554—

반응 단계

3.12 g of ethyl 2 -[4 -[((3S)-1-tert-butoxy-carbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetate was dissolved in 100 ml of tetrahydrofuran, followed by the addition of 4.65 g of (5-cyano-2-benzofuranyl)methyltriphenylphosphonium chloride. To the thus prepared solution was added 400 mg of 60% sodium hydride. With stirring, to the resulting mixture was added dropwise 3 ml of ethanol, followed by stirring at room temperature for 1 hour. The resulting reaction solution was neutralized with 10% citric acid solution, extracted with ethyl acetate, and then dried to distill off the solvent. Thereafter, the residue thus obtained was subjected to silica gel column chromatography using a toluene/ethyl acetate mixture as an elution solvent, thereby obtaining 3.1 g of ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(5-cyano-2-benzofuranyl)acrylate in the form of viscous oil as a mixture of E and Z forms. A portion of the thus obtained compound was separated into E and Z forms.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05866577
출처 데이터셋uspto-grants-1999_02
ORD IDord-795c793325ef45c486a007f251b35cdd
출처 메모uspto-grants-1999_02