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HRID 31344作成日:2026年10月23日

Tetrahydrofuran → 5-Chloro-3-hydroxy-3-(3-methoxyphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/ja/reaction/31344

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物3-BromoanisoleHCID 16971—
反応物Ammonium ChlorideHCID 25517—
反応物5-chloro-1H-indole-2,3-dioneHCID 87203—
反応物MagnesiumHCID 5462224—
生成物5-Chloro-3-hydroxy-3-(3-methoxyphenyl)-1,3-dihydro-2H-indol-2-oneHCID 22560825—
生成物HCID 178490745HCID 178490745—

反応手順

A solution of 3-methoxyphenylmagnesium bromide is prepared from 3.5 g of magnesium in 10 ml of THF and from a solution of 25 g of 1-bromo-3-methoxy-benzene in 40 ml of THF. This solution is added dropwise, under a nitrogen atmosphere, to a mixture of 8 g of 5-chloro-1H-indole-2,3-dione in 50 ml of THF, while keeping the temperature of the reaction medium below 40° C., followed by refluxing for 1 hour. The reaction mixture is cooled to RT, poured into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. 9.1 g of the expected product are obtained after crystallization from hot iso ether; m.p.=212° C.

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-1935a5b414384453ae3b0fd32dff8349
出典メモuspto-grants-2008_09