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HRID 2173422作成日:2026年10月26日

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

https://huagongshe.com/reaction/2173422

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Potassium vinyltrifluoroborateHCID 23679353—
反応物(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 71270763—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
生成物6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 67517715—

反応条件

温度100 °C

反応手順

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 Cl2Pd(dppf)2-DCM (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 6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-one. 1H NMR (500 MHz; CDCl3): 8.07 (d, J=8.0 Hz, 1H), 7.44 (dd, J=1.2, 7.1 Hz, 1H), 7.26 (s, 1H), 6.75 (dd, J=10.8, 17.6 Hz, 1H), 5.90 (d, J=17.6 Hz, 1H), 5.44 (d, J=11 Hz, 1H), 4.75 (m, 1H), 2.96 (m, 2H), 1.54 (d, J=6.1 Hz, 3H); LC/MS (M+H)+189;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09056859B2
出典データセットuspto-grants-2015_06
ORD IDord-43fe3ee364fc4a8d953f97a7e7aa1e00
出典メモuspto-grants-2015_06