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HRID 1295144作成日:2026年10月27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/1295144

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US07241789B2
出典データセットuspto-grants-2007_07
ORD IDord-449305433538438f85ec024d6cce68ae
出典メモuspto-grants-2007_07