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HRID 650405作成日:2026年10月25日

2-Bromoanisole → 1-(2-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid

https://huagongshe.com/reaction/650405

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromoanisoleHCID 11358—
反応物MagnesiumHCID 5462224—
反応物Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylateHCID 18427631—
反応物Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylateHCID 18969641—
反応物HCID 178489560HCID 178489560—
溶媒TetrahydrofuranHCID 8028—
溶媒Ether tetrahydrofuranHCID 21868444—
生成物1-(2-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acidHCID 18703900—

反応手順

Ethyl (1RS)-1-Hydroxy-1-(2-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate. To dry magnesium turnings (81 mg, 3,4 mmol) under an argon atmosphere was added a solution of 2-bromoanisole (0.64 g, 3.4 mmol) in 5:1 THF/Et2O (3 ml). A portion of the resulting 2-methoxyphenyl magnesium bromide solution (0.45 ml, 0.51 mmol) was added dropwise to a solution of ethyl 3-(3,4-methylenedioxyphenyl)-1-oxoindene-2-carboxylate (100 mg, 0.34 mmol) in THF (6 ml) under an argon atmosphere at 0° C. After stirring for 15 min, the mixture was partitioned between 3M HCl and EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3, H2O and saturated aqueous NaCl. The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 15% EtOAc/hexanes to afford the title compound. (100 mg, 68%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06271399B1
出典データセットuspto-grants-2001_08
ORD IDord-3c72d7f638d84ce8a77650922b6c27de
出典メモuspto-grants-2001_08