戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 517346作成日:2026年10月26日

Acetic Acid → 4-Ethoxycarbonylfuran-2-carboxylic acid

https://huagongshe.com/reaction/517346

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Hydrochloric AcidHCID 313—
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物TriphenylphosphineHCID 11776—
反応物BromineHCID 24408—
反応物Ethyl 3-furoateHCID 69201—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物4-Ethoxycarbonylfuran-2-carboxylic acidHCID 53429231—

反応手順

3-Furancarboxylic acid ethyl ester (1.4 g, 10.0 mmol) was dissolved in acetic acid (10 mL), bromine (1.6 g, 10.0 mmol) was added, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20). The obtained crude fraction was dissolved in N,N-dimethylformamide (15 mL), palladium acetate (0.18 g, 0.78 mmol), triphenylphosphine (0.41 g, 1.55 mmol), triethylamine (2.2 mL, 15.5 mmol), and water (0.7 mL, 38.8 mmol) were added, and the mixture was stirred at 80° C. overnight under a carbon monoxide atmosphere. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by high performance liquid chromatography to give the title compound (0.47 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115107B2
出典データセットuspto-grants-2015_08
ORD IDord-c374a461fb674ca48a3a55051d3c3d7a
出典メモuspto-grants-2015_08