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HRID 1095273作成日:2026年10月27日

3,4,5-Trimethoxyphenol → 2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalcone

https://huagongshe.com/reaction/1095273

反応式

関与物質

役割名称HCID仕込み量
反応物3,4,5-TrimethoxyphenolHCID 69505—
反応物3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 319463—
生成物2'-Hydroxy-4',5',6'-trimethoxy-4-nitrochalconeHCID 7276706922%

反応条件

温度80 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08138165B2
出典データセットuspto-grants-2012_03
ORD IDord-4049c48a3e50449dade86f120b203cfc
出典メモuspto-grants-2012_03