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HRID 650393作成日:2026年10月26日

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

https://huagongshe.com/reaction/650393

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromoanisoleHCID 7730—
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 178491912HCID 178491912—
溶媒Ether tetrahydrofuranHCID 21868444—
生成物1-(4-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acidHCID 1590850080%

反応手順

Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate, A solution of 4-bromoanisole (0.89 g, 5.0 mmol) in 9:1 Et2O/THF (10 ml) was added to magnesium turnings (0.105 g, 5.0 mmol), and the resulting mixture was allowed to stir for 30 min. The resultant 4-methoxyphenyl magnesium bromide was added dropwise to a solution of ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate (0.77 g, 2.4 mmol) in 10: 1 Et2O/ THF (55 ml) at 0° C. The resulting mixture was stirred at 0° C. for 1 h and was then partitioned between EtOAc and 1M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with 5% aqueous NaHCO3 and saturated aqueous NaCl and dried (MgSO4). The solvent was removed under reduced pressure, and the residue was purified by flash chromatography on silica gel, eluting with 10% EtOAc/hexanes to afford the title compound as a yellow glassy solid (0.80 g, 80%).

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-3b93513ab0c946c19a9596f01a049c04
出典メモuspto-grants-2001_08