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HRID 393663作成日:2026年10月24日

5-(Methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione → Methyl 4-(((2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)methyl)amino)-2-methoxybenzoate

https://huagongshe.com/ja/reaction/393663

反応式

関与物質

役割名称HCID仕込み量
反応物5-(Methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 152111—
反応物Methyl 4-amino-o-anisateHCID 168705—
溶媒IsopropanolHCID 3776—
生成物Methyl 4-(((2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)methyl)amino)-2-methoxybenzoateHCID 2264655796.4%

反応条件

温度50 °C

反応手順

3-Methoxy-4-methoxycarbonylaniline (14.15 g, 78 mmol) was suspended in isopropanol and heated at 50° C. 2,2-Dimethyl-5-methoxymethylene-1,3-dioxane-4,6-dione (14.8 g, 80 mmol), (Montatsh. Chem. 1967, 98, 564), was then added in portions over 10 minutes and the mixture was heated at reflux for 30 minutes. The mixture was left to cool to ambient temperature overnight. The precipitate formed was collected by filtration, washed with isopropanol and dried under vacuum to give 5-((3-methoxy-4-methoxycarbonylanilino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (25.2 g, 96%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809097B1
出典データセットuspto-grants-2004_10
ORD IDord-9924ef78b0284c45b6b40f18e00b8704
出典メモuspto-grants-2004_10