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HRID 19528作成日:2026年10月26日

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

https://huagongshe.com/reaction/19528

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 178478990HCID 178478990—
溶媒TetrahydrofuranHCID 8028—
生成物1-cyclohexyl-1-hydroxy-6-methoxy-3-phenyl-1H-indene-2-carboxylic acid ethyl esterHCID 1163975230.2%

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 (78 mg, 0.253 mmol) obtained in Example 1 was dissolved in THF, and 18%-cyclohexylmagnesium chloride (0.7 mL, 0.506 mmol) was added thereto, followed by stirring for 5 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 30 mg of the titled compound (yield: 30%).

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-7a10624842704a7abc2067372af0646d
出典メモuspto-grants-2010_06