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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572480생성일: 2026년 10월 26일

Nitrogen → (R)-3-(2-((tert-butyldiphenylsilyl)oxy)-1-hydroxyethyl)-4-(3,4-dimethylphenyl)-1H-isochromen-1-one

https://huagongshe.com/reaction/572480

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Sodium CarbonateHCID 10340—
반응물3,4-Dimethylphenylboronic acidHCID 2734348—
반응물(R)-4-bromo-3-(2-((tert-butyldiphenylsilyl)oxy)-1-hydroxyethyl)-1H-isochromen-1-oneHCID 68294919—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(R)-3-(2-((tert-butyldiphenylsilyl)oxy)-1-hydroxyethyl)-4-(3,4-dimethylphenyl)-1H-isochromen-1-oneHCID 8670071762%

반응 단계

A solution of 4-bromo-3-((1R)-2-{[(1,1-dimethylethyl)(diphenyl)silyl]oxy}-1-hydroxyethyl)-1H-2-benzopyran-1-one (142 mg, 0.271 mmol) and 3,4-dimethylphenylboronic acid (61.0 mg, 0.407 mmol) in N,N-Dimethylformamide (DMF) (2.5 mL) was degassed with N2 for 10 min. The reaction mixture was treated with 2M Na2CO3 (149 μl, 0.298 mmol) and Pd(PPh3)4 (16 mg, 0.014 mmol) and irradiated in the microwave for 20 min at 120° C. The reaction mixture was diluted with EtOAc, and washed with saturated aqueous NH4Cl, brine, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel chromatography (ethyl acetate-hexanes 0-30%) to afford the title compound (92 mg, 0.168 mmol, 62% yield) as a white solid: Rt=1.31, 1.33 (atropisomers), ES+ MS: 571 (M+23).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029391B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-73385b61a6f841aebf7c2ec077c97425
출처 메모uspto-grants-2015_05