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Benzaldehyde → 4-Butyl-2-phenyl-1,3-dioxolane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | 1,2-Hexanediol | HCID 94335 | — |
| 触媒 | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4-Butyl-2-phenyl-1,3-dioxolane | HCID 21710576 | 102.2% |
反応手順
A solution of benzaldehyde (5.1 mL, 50.0 mmol), 1,2-hexanediol (6.5 g, 55.0 mmol), and camphorsulfonic acid (0.58 g, 2.5 mmol) in 50 mL of toluene was heated to reflux (Dean-Stark) with azeotropic removal of water. When the theoretical amount of water was distilled (4.5 hours), the mixture was cooled to room temperature and diluted with 80 mL of ether. The solution was extracted with 2M aqueous sodium carbonate, water and brine, dried (Na2SO4), filtered, and concentrated to provide 10.54 g (102%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06277871B1 |
| 出典データセット | uspto-grants-2001_08 |
| ORD ID | ord-50e9d02e287546d8aa1ddab3807cf092 |
| 出典メモ | uspto-grants-2001_08 |