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HRID 63621作成日:2026年10月24日

Dichloromethane → 7-(furan-3-yl)-3,4-dihydro-2H-1-benzopyran-4-one

https://huagongshe.com/ja/reaction/63621

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium BicarbonateHCID 516892—
反応物2-(Furan-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 2773996—
反応物6-Bromo-1-tetraloneHCID 10105069—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物7-(furan-3-yl)-3,4-dihydro-2H-1-benzopyran-4-oneHCID 11859791983%

反応条件

温度100 °C

反応手順

To a solution of 6-bromo-1,2,3,4-tetrahydronaphthalen-1-one (1.5 g, 6.6 mmol) in dioxane (6 mL) was added 2-(furan-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.92 g, 9.9 mmol), Pd(dppf)Cl2.DCM (540 mg, 0.66 mmol) and sat. NaHCO3 (2 mL). The mixture was stirred at 100° C. for 4 h under nitrogen. The mixture was cooled to rt and diluted with EtOAc, filtered, and concentrated. The residue was purified by silica gel chromatography (4:1 PE:EtOAc) to give 1.18 g (83%) of the title compound as white solid. 1H NMR (400 MHz, CDCl3): δ 2.82 (2H, t, J=6.2 Hz), 4.56 (2H, t, J=6.4 Hz), 6.71 (1H, s), 7.07 (1H, s), 7.14 (1H, d, J=8.4 Hz), 7.50 (1H, s), 7.81 (1H, s), 7.88 (1H, d, J=8.4 Hz). [M+H] Calc'd for C13H10O3, 215. Found, 215.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447046B2
出典データセットuspto-grants-2016_09
ORD IDord-75d1b073b3e7499f9287b84fd8750187
出典メモuspto-grants-2016_09