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HRID 15722作成日:2026年10月24日

Sodium Hydroxide → ethyl [4-(4-methoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate

https://huagongshe.com/ja/reaction/15722

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物p-Aminophenylacetic acid ethyl esterHCID 225219—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-hydroxy-4-methoxynaphtho[2,3-c]furan-1(3H)-oneHCID 21079335—
溶媒DichloromethaneHCID 6344—
生成物ethyl [4-(4-methoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetateHCID 8661203454.5%

反応手順

3-Hydroxy-4-methoxynaphtho[2,3-c]furan-1(3H)-one (50 mg, 0.22 mmol) and ethyl 4-aminophenylacetate (47 mg, 0.26 mmol) in dichloromethane (5 ml) were stirred at room temperature under nitrogen for 1 hour. Sodium triacetoxyborohydride (138 mg, 0.66 mmol) was added and stirring continued for 24 h. The reaction was adjusted to pH14 with sodium hydroxide solution (2N) and extracted with dichloromethane (3×5 ml). The combined extracts were evaporated under vacuum and the residue triturated with cyclohexane/ether to give ethyl[4-(4-methoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate as a white solid (45 mg, 54%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732622B2
出典データセットuspto-grants-2010_06
ORD IDord-780617ed16d1496c8b8e69f04c32cc69
出典メモuspto-grants-2010_06