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p-Toluenesulfonic acid → 4-Methoxy-2,2-dimethyl-1,3-benzodioxole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 3-Methoxycatechol | HCID 13622 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 4-Methoxy-2,2-dimethyl-1,3-benzodioxole | HCID 15061094 | — |
反応手順
3-Methoxycatechol (25 g) was dissolved in benzene, and dimethoxyacetal (35 ml) and a catalytic amount of p-toluenesulfonic acid were added thereto, followed by heating at reflux for 6 hours. After being allowed to stand for cooling, the mixture was adjusted to alkaline with an aqueous solution of sodium hydroxide, followed by extraction with ether. The organic layer was washed with a saturated saline and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=99/1) to give Compound IIbk-a (19.4 g, 60.5%) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06514996B2 |
| 出典データセット | uspto-grants-2003_02 |
| ORD ID | ord-b56b9681518f4d3ebb66dfcc047e363d |
| 出典メモ | uspto-grants-2003_02 |