戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 610092作成日:2026年10月25日

2,3,4-Trimethoxybenzaldehyde → 5-Methoxy-2-methyl-1-(2,3,4-trimethoxybenzylidene)-3-indenyl acetic acid

https://huagongshe.com/reaction/610092

反応式

関与物質

役割名称HCID仕込み量
反応物2,3,4-TrimethoxybenzaldehydeHCID 75006—
反応物Sodium MethoxideHCID 10942334—
反応物Methyl 5-methoxy-2-methyl-3-indenylacetateHCID 53634864—
溶媒WaterHCID 962—
生成物5-Methoxy-2-methyl-1-(2,3,4-trimethoxybenzylidene)-3-indenyl acetic acidHCID 54456864—

反応手順

To a solution of methyl 5-methoxy-2-methyl-3-indenylacetate 8.7 g (0.037 mol) and 2,3,4-trimethoxybenzaldehyde, 7.99 g (1.1 equivalent) is added 16+ml (2.0+equivalents) of 25% methanolic sodium methoxide. The mixture is stirred at reflux under nitrogen for 2 hours. An equal volume of water is added dropwise and refluxing continues for 30 min. The solution is cooled, diluted with water and extracted with ether (3×). Residual ether is blown off with nitrogen, and then the aqueous solution is acidified with 50% glacial acetic acid. The precipitated product is collected and washed thoroughly with water. The crude product is crystallized to give 5-methoxy-2-methyl-1-(2,3,4-trimethoxybenzylidene)-3-indenyl-acetic acid. (R and R1 =H, R2 =OCH3, R3 and R4 =H, R5, R6 and R7 =OCH3, R8 =CH3, o=1, M=OH)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05998477
出典データセットuspto-grants-1999_12
ORD IDord-a17c83ad980a4d1bbe7e0d353b0a99aa
出典メモuspto-grants-1999_12