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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl 6-methyl-2-phenyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylate | HCID 15147475 | — |
| 반응물 | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | Methyl 6-bromomethyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate | HCID 10410300 | 66.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04727073 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-dcd8d2b7abf04ce0bdd51fdc309fc6a6 |
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| 출처 메모 | uspto-grants-1988_02 |
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