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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitrogen | HCID 947 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 3,4-Dimethylphenylboronic acid | HCID 2734348 | — |
| 반응물 | (R)-4-bromo-3-(2-((tert-butyldiphenylsilyl)oxy)-1-hydroxyethyl)-1H-isochromen-1-one | HCID 68294919 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (R)-3-(2-((tert-butyldiphenylsilyl)oxy)-1-hydroxyethyl)-4-(3,4-dimethylphenyl)-1H-isochromen-1-one | HCID 86700717 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09029391B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-73385b61a6f841aebf7c2ec077c97425 |
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| 출처 메모 | uspto-grants-2015_05 |
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