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HRID 31352作成日:2026年10月23日

2-Bromoanisole → 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/ja/reaction/31352

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Ammonium ChlorideHCID 25517—
反応物5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dioneHCID 2732752—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-oneHCID 2190589976.3%
生成物HCID 178489560HCID 178489560—

反応手順

A solution of 2-methoxyphenylmagnesium bromide is prepared starting with 1.9 g of magnesium in 4 ml of ether and a solution of 14.54 g of 1-bromo-2-methoxybenzene in 21 ml of ether. This solution is added dropwise, under an argon atmosphere, to a mixture of 5 g of 5-trifluoromethoxy-1H-indole-2,3-dione in 26 ml of THF, precooled on an ice bath, the resulting mixture is then heated at the reflux temperature of the ether for 1 hour 30 minutes and is allowed to cool to RT. The reaction mixture is poured slowly into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with 5% K2CO3 solution, with water and with saturated NaCl solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. 2.8 g of the expected product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425566B2
出典データセットuspto-grants-2008_09
ORD IDord-c0c9fcda8b5943aea3d4da63af3bb7f5
出典メモuspto-grants-2008_09