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HRID 733181作成日:2026年10月27日

2,2-Dimethyl-1,3-dioxane-4,6-dione → Ethyl 6-(benzyloxy)-3-oxohexanoate

https://huagongshe.com/reaction/733181

反応式

関与物質

役割名称HCID仕込み量
反応物2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
反応物2-DimethylaminopyridineHCID 21885—
反応物Isopropenyl chloroformateHCID 93846—
反応物Potassium bisulfateHCID 516920—
反応物4-(Benzyloxy)butanoic acidHCID 562201—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 6-(benzyloxy)-3-oxohexanoateHCID 10264779—

反応条件

温度0 °C

反応手順

4-Benzyloxybutyric acid (6.38 mL), Meldrum's acid (5.76 g) and dimethylaminopyridine (9.77 g) were dissolved in DCM (200 mL) and cooled to 0° C. A solution of isopropenyl chloroformate in dichloromethane (100 mL) was added dropwise and stirring at 0° C. continued for a further 2 h. Potassium hydrogen sulphate (200 mL of a 10% aqueous solution) was then added, the organic phase separated, dried over sodium sulphate, and evaporated under reduced pressure. The residue was dissolved in ethanol (200 mL) and heated at reflux overnight. Following cooling, the solvent was evaporated under reduced pressure and the resultant oil was purified by flash silica column chromatography. 6-Benzyloxy-3-oxo-hexanoic acid ethyl ester was isolated as an orange oil (8.53 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589095B2
出典データセットuspto-grants-2009_09
ORD IDord-89951e2fd3ce4e01a09824d7d1d6ead2
出典メモuspto-grants-2009_09