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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515757생성일: 2026년 10월 25일

Tributylamine → (E)-tert-butyl 3-(2-acetyl-5-chlorophenyl)acrylate

https://huagongshe.com/reaction/515757

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참여 물질

역할이름HCID투입량
반응물TributylamineHCID 7622—
반응물tert-Butyl acrylateHCID 15458—
반응물1-(2-Bromo-4-chlorophenyl)ethanoneHCID 4712644—
촉매PalladiumHCID 23938—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(E)-tert-butyl 3-(2-acetyl-5-chlorophenyl)acrylateHCID 8949988363.2%

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온도100 °C

반응 단계

To a degassed solution of 1-(2-bromo-4-chlorophenyl)ethanone (1.0 g, 4.28 mmol), tributylamine (2.041 mL, 8.57 mmol), and tert-butyl acrylate (1.255 mL, 8.57 mmol) in DMF (10 mL) was added palladium on carbon (0.456 g, 0.428 mmol) and Pd(OAc)2 (0.096 g, 0.428 mmol). The reaction mixture was warmed to 100° C. After 16 h, the reaction was cooled to rt. The reaction was filtered and the solid was rinsed with DMF. The filtrate was diluted with EtOAc, washed with H2O (2×), brine, dried over Na2SO4, filtered and concentrated. Purification by normal phase chromatography afforded Intermediate 4A (0.760 g, 63%), as a brown oil. MS (ESI) m/z: 225.0 (M-C4H8+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108951B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-e6109ceab95f42b99835a4e040a87c59
출처 메모uspto-grants-2015_08