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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41614생성일: 2026년 10월 25일

Methanol → Methyl 3-bromo-2-pyridinecarboxylate

https://huagongshe.com/reaction/41614

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sulfuric AcidHCID 1118—
반응물3-Bromopyridine-2-carboxylic AcidHCID 2050129—
생성물Methyl 3-bromo-2-pyridinecarboxylateHCID 12828946—

반응 단계

H2SO4 (1.2 mL, 23.4 mmol, 1.0 eq.) was added to a solution of 3-bromopyridine-2-carboxylic acid (4.7 g, 23.4 mmol, 1.0 eq.) in MeOH (50 mL). The resulting solution was stirred for 14 hours while the temperature was maintained at reflux in an oil bath. The mixture was cooled to room temperature and concentrated under vacuum. The residue was dissolved in EtOAc (50 mL) and the pH was adjusted to 10 with Na2CO3 (5 mol/L). The resulting solution was extracted with EtOAc (100 mL). The organic layer was washed with water (1×100 mL) and saturated aqueous NaCl (2×100 mL), dried over anhydrous Na2SO4 and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with EtOAc/PE (1:20) to yield 3-bromopyridine-2-carboxylic acid methyl ester (4.0 g) as a yellow liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530663B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-858c77e68f334259ae302203a2806b40
출처 메모uspto-grants-2013_09