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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7009생성일: 2026년 10월 23일

p-Toluenesulfonic acid → Methyl 3-bromo-2-fluorobenzoate

https://huagongshe.com/ko/reaction/7009

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Trimethyl orthoformateHCID 9005—
반응물3-Bromo-2-fluorobenzoic acidHCID 2736313—
용매MethanolHCID 887—
생성물Methyl 3-bromo-2-fluorobenzoateHCID 2158450584%

반응 단계

A solution of 3-bromo-2-fluorobenzoic acid (0.219 g, 1 mmol) in dry methanol (5 ml) under nitrogen was treated with trimethylorthoformate (0.22 ml, 2 mmol) and p-toluenesulfonic acid (catalytic amount), and then heated under reflux. After 16 h, the mixture was evaporated and the residue partitioned between water and Et2O. The organic layer was washed with sat. sodium hydrogen carbonate solution, water, brine, dried (MgSO4) and evaporated to give methyl 3-bromo-2-fluorobenzoate (0.195 g, 0.84 mmol, 84%): 1H NMR (CDCl3) δ 7.90–7.85 (m, 1H), 7.71–7.65 (m, 1H), 7.10 (dt, 1H, J=8.0, 1.0 Hz) and 3.94 (s, 3H): MS (EI) 232 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084168B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d6c9ebd1225d4262acc61210cf49b56e
출처 메모uspto-grants-2006_08