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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1371521생성일: 2026년 10월 25일

Methyl Acrylate → 3-[2-(tert-Butoxycarbonylamino-methyl)-phenyl]-acrylic acid methyl ester

https://huagongshe.com/reaction/1371521

반응식

참여 물질

역할이름HCID투입량
반응물Methyl AcrylateHCID 7294—
반응물2-Bromo-N-(tert-butoxycarbonyl)benzylamineHCID 7018300—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-[2-(tert-Butoxycarbonylamino-methyl)-phenyl]-acrylic acid methyl esterHCID 69219588—

반응 조건

온도80 °C

반응 단계

To compound of Step A (161.0 g, 561.8 mmol) in DMF (800 mL) is added methyl acrylate (58.0 g, 674.2 mmol), TEA (170.5 g, 1685.4 mmol) and dichlorobis(triphenylphosphine)palladium(II) (7.9 g, 11.2 mmol). The mixture is heated at 80° C. for about 32 hours. The mixture is cooled, diluted with 1000 mL of EtOAc and washed with 10% aqueous sodium bisulfate. The aqueous portion is extracted three times with EtOAc and the combined organics are dried (Na2SO4) and concentrated to dryness. The residue is dissolved in a small amount of DCM and filtered through 7 inch of silica gel in a 2 L sintered glass funnel eluting with 25% EtOAc/hexanes. The eluent is concentrated to dryness and recrystallized from EtOAc/hexanes to afford about 116.9 g (71%) of Step B compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157463B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-8afd36daa8f14f39b41258846cf77805
출처 메모uspto-grants-2007_01