関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3,4,5-Trimethoxyphenol | HCID 69505 | — |
| 反応物 | 3-(4-nitrophenyl)prop-2-enoyl Chloride | HCID 319463 | — |
| 生成物 | 2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalcone | HCID 72767069 | 22% |
反応手順
A mixture of 3,4,5-trimethoxyphenol (1.85 g, 10 mmol) and 4-nitrocinnamoyl chloride (2.11 g, 10 mmol) was dissolved in BF3-Et2O complex (10 ml) and heated to 80° C. for 10 min, and then quenched with excess of water. The aqueous layer was extracted with dichloromethane. The combined organic layer was concentrated and the residue was purified by column chromatography on silica gel (CH2Cl2:EtOAc:Hexane=1:1:3) gave 7a (0.79 g, 22%) and 7b (1.54 g, 43%). 1H NMR (400 MHz, CDCl3) μ 3.81 (s, 3H), 3.90 (s, 3H), 3.91 (s, 3H), 6.29 (s, 1H), 7.74 (d, J=8.8 Hz, 2H), 7.76 (d, J=16.0 Hz, 1H), 8.01 (d, J=16.0 Hz, 1H), 8.26 (d, J=8.8 Hz, 2H), 13.44 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08138165B2 |
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| 出典データセット | uspto-grants-2012_03 |
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| ORD ID | ord-4049c48a3e50449dade86f120b203cfc |
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| 出典メモ | uspto-grants-2012_03 |
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