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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4673생성일: 2026년 10월 23일

Tetrahydrofuran → 5-Bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine

https://huagongshe.com/ko/reaction/4673

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Potassium CarbonateHCID 11430—
반응물Phosphorus tribromideHCID 24614—
반응물5-Hydroxy-methyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidineHCID 70419877—
용매BenzeneHCID 241—
생성물5-Bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidineHCID 10430078—

반응 단계

To a solution of phosphorus tribromide (16.85 g) in a mixture of benzene (150 ml) and tetrahydrofuran (150 ml) was dropwise added a solution of 5-hydroxy-methyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine (30 g) in tetrahydrofuran (150 ml) under cooling at 7°-10° C. After stirring for 4 hours at the same temperature, the reaction mixture was poured into ice-water (200 ml), adjusted to pH 9.5 with saturated potassium carbonate and extracted with ethyl acetate (300 ml). After filtering off an insolble material, the organic layer was washed with saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from diethyl ether to give 5-bromomethyl-6-methyl-2-phenyl-4-(3-nitrophenyl)pyrimidine (29.08 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727073
출처 데이터셋uspto-grants-1988_02
ORD IDord-5445957897b14e47a375be80f7ca2538
출처 메모uspto-grants-1988_02