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HRID 586767作成日:2026年10月26日

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

https://huagongshe.com/reaction/586767

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Potassium CarbonateHCID 11430—
反応物Dibromoacetic AcidHCID 12433—
反応物2-Bromo-3,4-dihydroxybenzaldehydeHCID 13109575—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒1-PropanolHCID 1031—
生成物4-Bromo-5-formyl-benzo[1,3]dioxole-2-carboxylic acid methyl esterHCID 87578840—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06936719B2
出典データセットuspto-grants-2005_08
ORD IDord-671dd3dd86974b028e656e7c964c4937
出典メモuspto-grants-2005_08