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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273229생성일: 2026년 10월 24일

Sulfuric Acid → Methyl 5-bromo-2-iodobenzoate

https://huagongshe.com/ko/reaction/273229

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물N-bromobutanimideHCID 67184—
반응물Benzoic acid, 2-iodo-, methyl esterHCID 69132—
용매Acetic AcidHCID 176—
생성물Methyl 5-bromo-2-iodobenzoateHCID 11078356—

반응 단계

To a stirred slurry of methyl 2-iodo-benzoate (5.0 g, 0.019 mol) and N-bromosuccinimide (3.74 g, 0.021 mol) in acetic acid (10 mL) was added concentrated H2SO4 (10 mL) dropwise, keeping the temperature at 20-40° C. The mixture was stirred at room temperature for 88 hours and then heated at 50° C. for 4 hours. The mixture was cooled to 10° C., treated with 40 g of ice water, and extracted with 50 mL of CH2Cl2. The organic phase was washed in succession with 2×50 mL 5% NaHCO3, 50 mL 10% Na2S2O3, 50 mL water, and concentrated to colorless oil. The residue was purified by column chromatography (silica gel, 10:90 EtOAc:hexane) to provide the title compound. 1H NMR (CDCl3, 400 MHz) δ 7.92 (d, J=4 Hz, 1H), 7.83 (d, J=8 Hz, 1H), 7.27 (dd, J=8, 4 Hz, 1H), 3.92 (s, 3H); MS (DCl/NH3) [M+NH4]+ at 358, [M+NH3NH4]+ at 375.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456196B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-da2a2bebb8254deab543225f97e10220
출처 메모uspto-grants-2008_11