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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483803생성일: 2026년 10월 27일

Water → alpha,alpha-Bis(4-bromophenyl)-5-pyrimidinemethanol

https://huagongshe.com/reaction/483803

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4,4'-DibromobenzophenoneHCID 72868—
반응물5-BromopyrimidineHCID 78344—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물alpha,alpha-Bis(4-bromophenyl)-5-pyrimidinemethanolHCID 19043035—

반응 단계

A solution of 20 ml of 1.6N n-butyllithium in hexane is added dropwise within 30 minutes, with stirring and with the exclusion of moisture, to a solution, cooled to -75°, of 5.2 g (33 mmol) of 5-bromopyrimidine and 10.7 g (31.2 mmol) of 4,4'-dibromobenzophenone in 130 ml of THF. The reaction mixture is stirred for a further 0.5 hour at -75° and then for 16 hours at room temperature; then, while cooling with ice, it is hydrolysed by adding 20 ml of water. The organic phase is separated and diluted with ethyl acetate. The solution is washed with 2N HCl and a semi-saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated by evaporation. The residue is purified by column chromatography (400 g of silica gel, methylene chloride/ethyl acetate 85:15) and recrystallised from ethyl acetate, m.p. 89°-90°, Rf value=0.11 (silica gel, methylene chloride/ethyl acetate 85:15).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05227393
출처 데이터셋uspto-grants-1993_07
ORD IDord-d1218f6eacb444768780ec2eb689daa7
출처 메모uspto-grants-1993_07