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HRID 22590作成日:2026年10月26日

Ethylene Glycol → 2-(3-Ethenylphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/22590

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物WaterHCID 962—
反応物3-VinylbenzaldehydeHCID 39390—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒BenzeneHCID 241—
生成物2-(3-Ethenylphenyl)-1,3-dioxolaneHCID 10241313—

反応手順

To a solution of 3-ethenylbenzaldehyde from Step 1 (3.77 g) and ethylene glycol (1.8 mL) in benzene (40 mL) was added p-toluenesulfonic acid monohydrate (100 mg). The reaction mixture was heated to reflux for 6 hours. The water produced by the reaction was collected in a Dean-Stark trap. The reaction was allowed to cool to room temperature. The reaction was diluted with NH4OAc buffer and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated. Flash chromatography of the residue using 15% diethyl ether in hexane afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428171
出典データセットuspto-grants-1995_06
ORD IDord-587e164d49264c9ebf8e8b4e81762f69
出典メモuspto-grants-1995_06