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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1501958생성일: 2026년 10월 26일

2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl → (3R)-3-methyl-6-(prop-1-en-2-yl)-3,4-dihydro-1H-isochromen-1-one

https://huagongshe.com/reaction/1501958

반응식

참여 물질

역할이름HCID투입량
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 71270763—
반응물HCID 178456138HCID 178456138—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
생성물(3R)-3-methyl-6-(prop-1-en-2-yl)-3,4-dihydro-1H-isochromen-1-oneHCID 89619009—

반응 조건

온도0 °C

반응 단계

A 0.5 molar solution of zinc chloride (1.696 g, 12.44 mmol) in dry THF (16.59 mL) was cooled to 0° C. A solution of isopropenylmagnesium bromide (24.89 mL, 12.44 mmol) was added via syringe. The reaction was stirred at 0° C. for 30 minutes before being cannulated into a sealed tube containing (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one (2.00 g, 8.30 mmol), PdOAc2 (0.093 g, 0.42 mmol), and X—PHOS (0.395 g, 0.830 mmol) in THF (16.6 mL) under N2 atmosphere. The tube was heated to 70° C. overnight. The reaction was then cooled and partitioned between water (100 mL) and EtOAc (220 mL). The organic layer was then washed with brine, dried over magnesium sulfate, filtered and concentrated. MPLC purification (10-50% EtOac/Hex) gave (3R)-3-methyl-6-(prop-1-en-2-yl)-3,4-dihydro-1H-isochromen-1-one:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206199B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-287c85a584e84c2bb447152dd826e36e
출처 메모uspto-grants-2015_12