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HRID 53285作成日:2026年10月24日

Hexane → Methyl 4-[2-(1,1-dimethyl-3-oxo-indan-5-yl)vinyl]benzoate

https://huagongshe.com/ja/reaction/53285

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 4-ethenylbenzoateHCID 583124—
反応物6-bromo-3,3-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 10776365—
触媒palladium(II) acetateHCID 167845—
触媒Tetrabutylammonium chloride hydrateHCID 16212273—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 4-[2-(1,1-dimethyl-3-oxo-indan-5-yl)vinyl]benzoateHCID 5433662270%

反応手順

6-Bromo-3,3-dimethyl-indan-1-one (1.20 g, 5.02 mmol), methyl 4-vinylbenzoate (1.63 g, 10.0 mmol), palladium acetate (56 mg, 0.25 mmol), tetrabutylammonium chloride hydrate (1.53 g, 5.52 mmol ), and sodium bicarbonate (1.05 g, 12.6 mmol) were stirred in 10 mL of anhydrous N,N-dimethylformamide at 80°-100° C. for 8 hours. The mixture was diluted with water (100 mL), extracted with methylene chloride (50 mL×3). The combined extracts were dried over magnesium sulfate and evaporated. The residue was purified by flash chromatography (CH2Cl2 :hexane=1:1 to 1:0, then CH2Cl2 :EtOAc=10:1) to give 1.12 g (70% yield) of the title compound as a yellow solid; 1H-NMR (CDCl3) δ1.45 (s, 6H), 2.64 (s, 2H), 5.30 (s, 3H), 7.18 (d, J=16.5 Hz, 1H), 7.26 (d, J=16.5 Hz, 1H), 7.52 (d, J=8.1 Hz, 1H), 7.58 (d, J=8.5 Hz, 2H), 7.78 (d, J=1.7, 8.1 Hz, 1H), 7.86 (d, J=1.7 Hz, 1H), 8.05 (d, J=8.5 Hz, 2H); MS m/e 321 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618839
出典データセットuspto-grants-1997_04
ORD IDord-e894fad907b74d91b47cdd45f501a1db
出典メモuspto-grants-1997_04