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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1501945생성일: 2026년 10월 27일

Triethylamine → (3R)-6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-one

https://huagongshe.com/reaction/1501945

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium vinyltrifluoroborateHCID 23679353—
반응물(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 71270763—
촉매HCID 178418807HCID 178418807—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물(3R)-6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 86727028—

반응 조건

온도100 °C

반응 단계

A solution of (3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one (2.4 g, 9.96 mmol) and triethylamine (2.78 mL, 19.91 mmol) in EtOH (39.8 mL) was added to a microwave vial containing PdCl2(dppf)-CH2Cl2, (0.406 g, 0.498 mmol) and potassium vinyltrifluoroborate (2.000 g, 14.93 mmol). The contents of the vial were heated to 100° C. for 1 hour after which the mixture was cooled, diluted with chloroform (50 mL) and washed with aqueous ammonium chloride (25 mL). The organic layer was then dried over magnesium sulfate, filtered and the solvent was evaporated under reduced pressure. MPLC purification (15-60% EtOAc/Hex) gave the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206199B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-75f27879dd2c4c20a5a8b4bb2c8a7392
출처 메모uspto-grants-2015_12