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HRID 372085作成日:2026年10月26日

Benzenepropanal → 2-(2-Phenylethyl)oxirane

https://huagongshe.com/reaction/372085

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenepropanalHCID 7707—
反応物Sodium hydrideHCID 24758—
反応物Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
反応物HCID 178418361HCID 178418361—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2-Phenylethyl)oxiraneHCID 135955—

反応手順

A solution of trimethyloxosulphonium iodide (2.64 g.) in dry dimethylsulphoxide (50 ml.) is stirred at 50°-60° C. in an atmosphere of nitrogen and an 80% w/w mineral oil dispersion of sodium hydride (0.36 g.) is added. Stirring and heating are continued until the solution is clear and no more hydrogen is evolved. A solution of 3-phenylpropionaldehyde (1.34 g.) in dry dimethyl sulphoxide (10 ml.) is added and the mixture is stirred at 50°-60° C. in an atmosphere of nitrogen for 3 hours. The mixture is cooled and diluted with water (200 ml.), and the product is obtained by extraction with ethyl acetate (3 × 80 ml.). Removal of the solvent from the combined extracts gives 1,2-epoxy-4-phenylbutane as an oil which is not further purified.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04088814
出典データセットuspto-grants-1978_05
ORD IDord-21c9243e88074b5e9e017892ae3176f7
出典メモuspto-grants-1978_05