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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47911생성일: 2026년 10월 26일

Sulfuric Acid → 4-Bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/47911

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Potassium CarbonateHCID 11430—
반응물Dibromoacetic AcidHCID 12433—
반응물2-Bromo-3,4-dihydroxybenzaldehydeHCID 13109575—
용매MethanolHCID 887—
용매WaterHCID 962—
용매1-PropanolHCID 1031—
생성물4-Bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid methyl esterHCID 87578840—

반응 단계

To a mixture of 2-bromo-3,4-dihydroxy-benzaldehyde (2.17 g, 10.0 mmol) and K2CO3 (5.56 g, 40.2 mmol) in n-propanol (25 mL) was added dibromoacetic acid (2.18, 10.0 mmol) and the mixture was heated at reflux temperature for 24 h. After cooling to room temperature, another portion of dibromoacetic acid (1.75 g, 8.0 mmol) was added. The mixture was stirred at reflux for 46 h. n-Propanol was evaporated and water (30 mL) was added. The resulting aqueous solution was acidified to pH 2 by adding 1 N HCl and extracted with ethyl acetate (3×100 mL). The combined organic layers were dried (MgSO4) and evaporated in vacuo to afford crude 4-bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid (1.34 g) as a brownish solid. This crude product was dissolved in anhydrous methanol (50 mL) and conc. H2SO4 (5 mL) was added drop by drop. The resulting mixture was refluxed overnight and cooled to room temperature. Water (50 mL) was added and the resulting aqueous solution was extracted with ethyl acetate (100 mL×3). The combined organic layers were dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (ethyl acetate:hexane=5:95) to furnish 4-bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid methyl ester as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699994B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-6a88c84769cd4133add1015337f6909e
출처 메모uspto-grants-2004_03