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HRID 4511생성일: 2026년 10월 23일

Ammonium Chloride → Methanone,(2,4-dichlorophenyl)-5-pyrimidinyl-

https://huagongshe.com/ko/reaction/4511

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Methyl 2,4-dichlorobenzoateHCID 37055—
반응물5-BromopyrimidineHCID 78344—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Methanone,(2,4-dichlorophenyl)-5-pyrimidinyl-HCID 14719595—

반응 단계

61.8 g (0.3 mole) of methyl 2,4-dichlorobenzoate and 52.2 g (0.33 mole) of 5-bromopyrimidine are dissolved in a mixture of 400 ml of tetrahydrofuran and 200 ml of diethyl ether. After the addition of 30 g of molecular sieve, the reaction mixture is stirred for 1/2 hour at room temperature and then cooled to about -120° C. 187.2 ml (0.3 mole) of butyl lithium as a 1.6 molar solution in hexane are added dropwise at this temperature. The reaction mixture is then stirred for 11/2 hours in the temperature range from -100° to -130° C. Subsequently, while allowing the temperature to increase to room temperature, stirring is continued until the reaction is complete. 300 ml of 10% ammonium chloride solution are then added dropwise, and the reaction mixture is extracted three times with ethyl acetate. The organic solution is dried over sodium sulfate and then filtered, and the filtrate is concentrated. The resultant crude product is then purified through a flash column packed with silica gel (eluant: a 3:1 mixture of petroleum ether and ethyl acetate), affording 45 g (59.3% of theory) of the title compound with a melting point of 75°-78° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727075
출처 데이터셋uspto-grants-1988_02
ORD IDord-ecedeae11bc2433581aed340c21acce6
출처 메모uspto-grants-1988_02