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HRID 19527作成日:2026年10月27日

Ethyl 6-methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylate → 1-benzyl-1-hydroxy-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/19527

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 6-methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylateHCID 23249734—
反応物HCID 178418336HCID 178418336—
溶媒TetrahydrofuranHCID 8028—
生成物1-benzyl-1-hydroxy-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl esterHCID 1156752913%

反応条件

温度0 °C

反応手順

6-Methoxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid ethyl ester (300 mg, 0.974 mmol) obtained in Example 1 was dissolved in THF and 1.2 equivalents of benzylmagnesium chloride were added thereto, followed by stirring for 3 hrs at 0° C. The resulting mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4, and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 50 mg of the titled compound (yield: 13%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745439B2
出典データセットuspto-grants-2010_06
ORD IDord-12735fdaa0834c919d6824b5a1075a62
出典メモuspto-grants-2010_06