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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7054생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Homovanillic AcidHCID 1738—
반응물PentafluorophenolHCID 13041—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매DichloromethaneHCID 6344—
생성물4-Hydroxy-3-methoxyphenylacetic acid pentafluorophenyl esterHCID 2250738098.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084176B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b2a4ac5e1aac4e2bbc9b719031e51886
출처 메모uspto-grants-2006_08