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HRID 218528作成日:2026年10月25日

Sodium Chloride → 1-(2-Bromo-4-nitrophenyl)tetrahydropyrimidin-2(1H)-one

https://huagongshe.com/reaction/218528

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
反応物2(1H)-Pyrimidinone, tetrahydro-HCID 74615—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1-(2-Bromo-4-nitrophenyl)tetrahydropyrimidin-2(1H)-oneHCID 59586715—

反応手順

910 mg (9.09 mmol) of tetrahydropyrimidinone in 39 ml of DMSO are admixed at RT with 1.53 g (13.6 mmol) of potassium tert-butoxide, and the mixture is stirred at room temperature for 30 min. 2.00 g (9.09 mmol) of 2-bromo-1-fluoro-4-nitrobenzene are added and the mixture is stirred at 60° C. After 18 h, it is cooled and added to 600 ml of water and 160 ml of saturated aqueous sodium chloride solution. It is extracted three times with 300 ml each time of ethyl acetate, and the combined organic phases are dried over sodium sulfate. After filtration, the solvents are removed under reduced pressure and the residue is purified by chromatography on silica gel (60:1 dichloromethane/ethanol). This affords 481 mg (17% of theory) of the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198267B2
出典データセットuspto-grants-2012_06
ORD IDord-9f39347d968c465b9431cc946213fff9
出典メモuspto-grants-2012_06