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p-Toluenesulfonic acid → HCID 60077026、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Methyl (4R)-2,2-dimethyl-1,3-dioxolane-4-carboxylate | HCID 853166 | — |
| 反応物 | HCID 10866664 | HCID 10866664 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 60077026 | HCID 60077026 | 81% |
反応手順
To a solution of methyl-α,β-isopropylidene-D-glycerate (II) (Fluka: registry # 52373-72-5), (9.76 g, 60.9 mmol, 1 eq) and benzoyloxyacetaldehyde I (10 g, 60.9 mmol, 1 eq) in toluene (20 mL) at 80° C., p-toluenesulfonic acid (PTSA) (460 mg, 2.4 mmol, 4 mol %) was added. The reaction flask was kept under vacuum for one hour and a distillate was collected (80-85° C.) during this period of time. The residue was then cooled to room temperature (RT) and purified by column chromatography on silica gel, using hexanes/ethyl acetate as eluent to produce 13.2 g (81%) of the title compound as a mixture of cis and trans isomers in a ratio of 3:1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06566365B1 |
| 出典データセット | uspto-grants-2003_05 |
| ORD ID | ord-c47028294e8d4dbdadf4c702b7dd847c |
| 出典メモ | uspto-grants-2003_05 |