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HRID 1057941作成日:2026年10月27日

p-Toluenesulfonic acid → 4-Methoxy-2,2-dimethyl-1,3-benzodioxole

https://huagongshe.com/reaction/1057941

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物3-MethoxycatecholHCID 13622—
反応物Sodium HydroxideHCID 14798—
溶媒BenzeneHCID 241—
生成物4-Methoxy-2,2-dimethyl-1,3-benzodioxoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06514996B2
出典データセットuspto-grants-2003_02
ORD IDord-b56b9681518f4d3ebb66dfcc047e363d
出典メモuspto-grants-2003_02