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Ethylene Glycol → 2-(3-Ethenylphenyl)-1,3-dioxolane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethylene Glycol | HCID 174 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | 3-Vinylbenzaldehyde | HCID 39390 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 2-(3-Ethenylphenyl)-1,3-dioxolane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05428171 |
| 出典データセット | uspto-grants-1995_06 |
| ORD ID | ord-587e164d49264c9ebf8e8b4e81762f69 |
| 出典メモ | uspto-grants-1995_06 |