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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 3-(5-Benzyloxy-indol-1-yl)-3-phenyl-acrylic acid ethyl ester | HCID 67427786 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(5-Hydroxy-indol-1-yl)-3-phenyl-propionic acid ethyl ester | HCID 66821478 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06855722B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-45016ebf77d4465093ab94320b8e0a61 |
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| 出典メモ | uspto-grants-2005_02 |
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