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HRID 24005作成日:2026年10月25日

3-(5-Benzyloxy-indol-1-yl)-3-phenyl-acrylic acid ethyl ester → 3-(5-Hydroxy-indol-1-yl)-3-phenyl-propionic acid ethyl ester

https://huagongshe.com/reaction/24005

反応式

関与物質

役割名称HCID仕込み量
反応物3-(5-Benzyloxy-indol-1-yl)-3-phenyl-acrylic acid ethyl esterHCID 67427786—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物3-(5-Hydroxy-indol-1-yl)-3-phenyl-propionic acid ethyl esterHCID 6682147896%

反応手順

A mixture of 3-(5-benzyloxy-indol-1-yl)-3-phenyl-acrylic acid ethyl ester (1.94 g, 4.89 mmol) and palladium on carbon [10% w/w] (60 mg) in methanol (25 mL) was stirred under hydrogen atmosphere for 24 h. After removal of the catalyst by filtration, the crude product was purified by flash chromatography on silica gel with hexane/ethyl acetate (4:1) to give the title compound in 96% yield. 1H NMR (CDCl3) δ 7.10-7.30 (m, 7H), 6.99 (d, J=2.4 Hz, 1H), 6.69 (dd, J=2.4 and 8.7 Hz, 1H), 6.39 (d, J=3.2 Hz, 1H), 5.99 (t, J=7.6 Hz, 1H), 5.31 (br, 1H), 4.03 (q, J=7.2 Hz, 2H), 3.26 (m, 2H), 1.08 (t, J=7.2 Hz, 3H). 13C NMR (CDCl3) δ 170.4, 149.7, 139.8, 131.5, 129.3, 128.8, 127.9, 126.2, 125.8, 111.6, 110.6, 105.2, 101.4, 61.1, 56.2, 40.4, 13.9. Mass Spectrum (LCMS, ESI) calculated for C19H20NO3 310.1 (M+H); found 310.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855722B2
出典データセットuspto-grants-2005_02
ORD IDord-45016ebf77d4465093ab94320b8e0a61
出典メモuspto-grants-2005_02