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HRID 7054作成日:2026年10月23日

Homovanillic Acid → 4-Hydroxy-3-methoxyphenylacetic acid pentafluorophenyl ester

https://huagongshe.com/ja/reaction/7054

反応式

関与物質

役割名称HCID仕込み量
反応物Homovanillic AcidHCID 1738—
反応物PentafluorophenolHCID 13041—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒DichloromethaneHCID 6344—
生成物4-Hydroxy-3-methoxyphenylacetic acid pentafluorophenyl esterHCID 2250738098.2%

反応手順

A mixture of 4-hydroxy-3-methoxyphenylacetic acid (4.65 g), pentafluorophenol (4.2 g), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (4.9 g) and methylene chloride (50 ml) was stirred at room temperature for 18 hours. The reaction solution was washed with water, and the organic layer was dried over sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give 4-hydroxy-3-methoxyphenylacetic acid pentafluorophenyl ester (7.8 g). This product is dissolved in ethyl acetate (80 ml), and thereto is added 3-iodeaniline (7.4 g). The mixture is heated at 60° C. under stirring for 18 hours. The solvent is evaporated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (6.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084176B2
出典データセットuspto-grants-2006_08
ORD IDord-b2a4ac5e1aac4e2bbc9b719031e51886
出典メモuspto-grants-2006_08