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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4682생성일: 2026년 10월 24일

Methyl 6-methyl-2-phenyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylate → Methyl 6-bromomethyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate

https://huagongshe.com/ko/reaction/4682

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 6-methyl-2-phenyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylateHCID 15147475—
반응물Acetic Acid Mixture with Hydrobromic AcidHCID 21893785—
용매Acetic AcidHCID 176—
생성물Methyl 6-bromomethyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylateHCID 1041030066.4%

반응 단계

A mixture of methyl 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate (5 g), pyridinium bromide perbromide (5.6 g) and 25% hydrogen bromide-acetic acid (5 ml) in acetic acid (200 ml) was stirred for 2 hours at room temperature. The reaction mixture was poured into ice water (200 ml) and stirred for 10 minutes. The resulting precipitates were collected and dissolved in a mixture of chloroform (50 ml) and water (50 ml). The separated organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride successively, dried over magnesium sulfate. The solvent was evaporated in vacuo and the residual crystal was recrystallized from ethanol to give methyl 6-bromomethyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate (4.07 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727073
출처 데이터셋uspto-grants-1988_02
ORD IDord-dcd8d2b7abf04ce0bdd51fdc309fc6a6
출처 메모uspto-grants-1988_02