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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11919생성일: 2026년 10월 24일

Ethyl Acrylate → (4R,9aR)-6-(2-Ethoxycarbonyl-vinyl)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/11919

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcrylateHCID 8821—
반응물Tri-o-tolylphosphineHCID 80271—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium AcetateHCID 517045—
반응물(4R,9aR)-6-bromo-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 86590113—
촉매Palladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
용매TolueneHCID 1140—
생성물(4R,9aR)-6-(2-Ethoxycarbonyl-vinyl)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 6955765391.2%

반응 단계

To a solution of 1.0 g (2.71 mmol) (4R,9aR)-6-bromo-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester (Example 5, intermediate b) and 0.36 ml (3.25 mmol) ethyl acrylate in 30 ml toluene were added 0.67 g (8.15 mmol) sodium acetate, 82.6 mg (0.27 mmol) tri(o-tolyl)phosphine and 0.04 mg (0.1 mmol) allylpalladium chloride dimer. The reaction mixture was heated under reflux for 20 h, then poured into saturated aqueous sodium bicarbonate solution and extracted with ethyl acetate. The organic phase was washed with 10% aqueous citric acid solution and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by column chromatography on silica gel (0.032–0.063 mm) with n-hexane:ethyl acetate (9:1) as eluant to afford the desired compound as a yellow solid (91.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098337B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-c7a4f3c997774bd4bc1869e396fb93b7
출처 메모uspto-grants-2006_08