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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537910생성일: 2026년 10월 26일

(4-Methoxyphenyl)boronic acid → 4-(4-methoxyphenyl)-5,5-dimethylfuran-2(5H)-one

https://huagongshe.com/reaction/537910

반응식

참여 물질

역할이름HCID투입량
반응물(4-Methoxyphenyl)boronic acidHCID 201262—
반응물Potassium FluorideHCID 522689—
반응물2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonateHCID 58926348—
촉매Benzyl triethylammonium chlorideHCID 66133—
촉매HCID 178418476HCID 178418476—
용매Toluene waterHCID 22272177—
생성물4-(4-methoxyphenyl)-5,5-dimethylfuran-2(5H)-oneHCID 58926254—

반응 조건

온도50 °C

반응 단계

To a 1:1 mixture of toluene/water (20 mL), were added 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate (100 mg, 0.38 mmol), 4-methoxyphenylboronic acid (87 mg, 0.57 mmol), PdCl2(PPh3)2 (27 mg, 0.038 mmol), 2M KF aqueous solution (0.95 mL, 1.9 mmol), benzyltriethylammonium chloride (8.7 mg, 0.038 mmol). The mixture was heated at 50° C. under N2 for 30 minutes, cooled to room temperature and extracted with EtOAc (2×50 mL). The organic layers were combined, washed with saturated NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4. Purification through silica gel column with 10-30% EtOAc/hexanes led to the product as yellow solid. Yield: 33 mg, 40%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865682B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-aadd9604ff304cf5bcfa0cfedf43042e
출처 메모uspto-grants-2014_10