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HRID 14463作成日:2026年10月25日

Benzyl Bromide → 7-Benzyloxy-3-(4-chlorophenyl)-2-isopropyl-4-oxo-4H-chromene-8-carbaldehyde

https://huagongshe.com/reaction/14463

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehydeHCID 86625608—
溶媒DimethylformamideHCID 6228—
生成物7-Benzyloxy-3-(4-chlorophenyl)-2-isopropyl-4-oxo-4H-chromene-8-carbaldehydeHCID 11510307—

反応手順

To a solution of 3-(4-chlorophenyl)-7-hydroxy-2-isopropyl-4-oxo-4H-chromene-8-carbaldehyde (7.95 g, 23.2 mmol) and benzyl bromide (7.93 g, 46.4 mmol) in N,N-dimethylformamide (200 ml) is added K2CO3 (9.61 g, 69.5 mmol), and the reaction mixture is stirred at room temperature for 96 h. The mixture is poured into ice/water, extracted with CH2Cl2, dried (MgSO4) and concentrated in vacuo. The resulting solid residue is stirred with hexane/ethyl acetate for 1 h, the solvent is decanted, and the solid is stirred with hexane/diethyl ether for 16 h. The title compound is collected by filtration and washed with hexane to afford a pale brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732435B2
出典データセットuspto-grants-2010_06
ORD IDord-7bde9c9bba4e4621a41a66b8d2eaf9a1
出典メモuspto-grants-2010_06