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HRID 1528034作成日:2026年10月25日

4-Bromo-2-methylbut-1-ene → 2-Methoxy-1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone

https://huagongshe.com/reaction/1528034

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-2-methylbut-1-eneHCID 549585—
反応物2-Methoxy-1-(2,4,6-trihydroxyphenyl)ethanoneHCID 643400—
溶媒Potassium HydroxideHCID 14797—
生成物2-Methoxy-1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanoneHCID 8670221541%

反応手順

2-methoxy-1-(2,4,6-trihydroxyphenyl)ethanone (8.3 g, 42 mmol) was dissolved in a 5% potassium hydroxide aqueous solution (84 ml). After the reaction mixture was cooled below 0° C., Isopentenyl bromide (12.48 g, 84 mmol) was slowly added dropwise to within 30 minutes. The reaction mixture was stirred at room temperature (RT) for 2 hours, then poured into an ice water and acidified to pH 2. The reaction mixture was extracted with ethyl acetate. The extract was collected and dried over anhydrous sodium sulfate, followed by removing solvent. The desired compound was obtained by purifying the residue by silica gel column chromatography (dichloromethane as eluent) (5.7 g, yield 41%). 1H NMR (400 MHz, DMSO-d6): δ=11.44 (s, 2H), 9.24 (s, 1H), 5.00 (t, 2H, J=6.8 Hz), 4.63 (s, 2H,), 3.31 (s, 3H), 3.22 (d, 4H, J=6.8 Hz), 1.67 (s, 6H), 1.58 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09090583B2
出典データセットuspto-grants-2015_07
ORD IDord-53f269416ed1433b81d3fd78cfd8b932
出典メモuspto-grants-2015_07