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p-Toluenesulfonic acid → (2S,4R)-4-(Bromomethyl)-2-(Diethoxyphosphinoylmethyl)-1,3-Dioxolane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Diethyl (2,2-diethoxyethyl)phosphonate | HCID 82071 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (2R)-3-Bromo-1,2-propanediol | HCID 2733893 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (2S,4R)-4-(Bromomethyl)-2-(Diethoxyphosphinoylmethyl)-1,3-Dioxolane | HCID 53652584 | 97% |
反応手順
To a solution of diethylphosphonoacetaldehyde diethylacetal (4.20 g, 16.5 mmol) and (2R)-3-bromo-1,2-propanediol (example 90) (3.00 g, 19.4 mmol, 1.2 eq.) in toluene (30 mL) was added pTSA (few crystals). The mixture was stirred at reflux for 50 hr. After, the solution was cooled to room temperature, and a saturated solution of sodium bicarbonate was added, and the aqueous phase was extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulphate and evaporated under reduced pressure. The crude material was pure by TLC and NMR, and gave 5.06 g of the compound in a 97% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06127540 |
| 出典データセット | uspto-grants-2000_10 |
| ORD ID | ord-165cb66a52b34f6cbfccbcc9487ca69c |
| 出典メモ | uspto-grants-2000_10 |