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HRID 490144作成日:2026年10月26日

Ammonium Chloride → 3-(2-fluorophenyl)-3-hydroxy-5-(trifluoromethyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/490144

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1,1-Dimethylethyl N-[4-(trifluoromethyl)phenyl]carbamateHCID 11230745—
反応物Ethyl 2-(2-fluorophenyl)-2-oxoacetateHCID 21644544—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Cyclohexane hexaneHCID 22494920—
生成物3-(2-fluorophenyl)-3-hydroxy-5-(trifluoromethyl)-1,3-dihydro-2H-indol-2-oneHCID 2312069516.3%

反応条件

温度-40 °C

反応手順

16.8 mL of a hexane-cyclohexane solution of 1.0 mol/L sec-butyllithium was added dropwise under −78° C. cooling to a 15 mL tetrahydrofuran solution of 2 g of tert-butyl[4-(trifluoromethyl)phenyl]carbamate, and the reaction mixture was stirred for 1 hour. The temperature was then raised to −40° C., and the reaction mixture was stirred for 2.5 hours at that temperature. The reaction mixture was cooled back down to −78° C., a 7.5 mL tetrahydrofuran solution of 2.23 g of ethyl(2-fluorophenyl)(oxo)acetate was added dropwise, and the reaction mixture was stirred for 2 hours at the same temperature. The temperature was then raised to room temperature, and the reaction mixture was stirred for 12 hours. A saturated ammonium chloride aqueous solution was added to the reaction solution, extraction was performed with ethyl acetate, the organic layer was washed with saturated brine and dried with magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography (silica gel 60, mobile phase: ethyl acetate/hexane=1/1; v/v) to obtain 389 mg of the titled compound (colorless powder).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528124B2
出典データセットuspto-grants-2009_05
ORD IDord-39d2f4d5b355497d89243307d32f3284
出典メモuspto-grants-2009_05