戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 75153作成日:2026年10月25日

Pyridine → 2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dione

https://huagongshe.com/reaction/75153

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
反応物Isovaleryl chlorideHCID 66054—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dioneHCID 59437173113,914.297%

反応条件

温度0 °C

反応手順

To a solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (14.4 g, 0.1 mol) and pyridine (19.4 mL) in CH2Cl2 (150 mL) at 0° C., a solution of 3-methylbutyryl chloride (12 g, 0.1 mmol) in CH2Cl2 (140 mL) was added slowly. The reaction mixture was stirred for 1 h at 0° C. and for a further 1 h at rt. The mixture was concentrated to give a residue, which was diluted with EtOAc (500 mL) and filtered. The filtrate was washed with 10% aq Na2CO3 (200 mL) and water (200 mL). The combined aqueous layers were extracted with EtOAc (100 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4 and concentrated to give crude 5-(3-methylbutanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (26 g), which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835426B2
出典データセットuspto-grants-2014_09
ORD IDord-be324dd320404bf09b4b00ea3f374084
出典メモuspto-grants-2014_09