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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 631965생성일: 2026년 10월 25일

Phosphorus oxychloride → Methyl 5-bromo-6-chloropicolinate

https://huagongshe.com/reaction/631965

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참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Methyl 5-bromopyridine-2-carboxylateHCID 7016458—
반응물5-Bromo-2-(methoxycarbonyl)pyridine 1-oxideHCID 68458381—
용매DichloromethaneHCID 6344—
생성물Methyl 5-bromo-6-chloropicolinateHCID 4631119759%

반응 조건

온도60 °C

반응 단계

A mixture of 5-bromo-pyridine-2-carboxylic acid methyl ester (CAN 29682-15-3, 50 g, 0.23 mol) and m-CPBA (CAN 937-14-4, 80 g, 0.46 mol) in 400 mL dry methylene chloride was heated to 60° C. for 20 h. After that, the mixture was quenched with saturated sodium sulfite solution and extracted with ethyl acetate (2×200 mL). The organic layer was washed with brine (2×200 mL) and evaporated to dryness. The residue was purified by column chromatography (silica gel, 300 g, eluting with 15% ethyl acetate in petroleum ether) to obtain a brown oil. The brown oil, 5-bromo-2-(methoxycarbonyl)pyridine 1-oxide (30 g, 0.13 mol) was added into phosphoryl trichloride (CAN 10025-87-3, 80 mL) at 0° C. over 1 h, then the mixture was heated to 95° C. for 1 h. After that the mixture was evaporated to dryness, the residue was dissolved in water (50 mL), extracted with ethyl acetate (3×50 mL) and the organic layer was evaporated to dryness to obtain the product as a white solid (19 g, 59%); MS (EI): m/e=249.9 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321727B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-913a99fef4ba4cdeb75c356dd6c5f191
출처 메모uspto-grants-2016_04