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HRID 83695作成日:2026年10月26日

1-(4-Methoxyphenyl)cyclopropane-1-carboxylic acid → Methyl 1-(4-methoxyphenyl)-cyclopropanecarboxylate

https://huagongshe.com/reaction/83695

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Methoxyphenyl)cyclopropane-1-carboxylic acidHCID 85575—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒MethanolHCID 887—
生成物Methyl 1-(4-methoxyphenyl)-cyclopropanecarboxylateHCID 137075441,980.2%

反応手順

To a solution of 1-(4-methoxy-phenyl)-cyclopropanecarboxylic acid (50.0 g, 0.26 mol) in MeOH (500 mL) was added toluene-4-sulfonic acid monohydrate (2.5 g, 13.1 mmol) at room temperature. The reaction mixture was heated at reflux for 20 hours. MeOH was removed by evaporation under vacuum and EtOAc (200 mL) was added. The organic layer was washed with sat. aq. NaHCO3 (100 mL) and brine, dried over anhydrous Na2SO4 and evaporated under vacuum to give 1-(4-methoxy-phenyl)-cyclopropanecarboxylic acid methyl ester (53.5 g, 99%). 1H NMR (CDCl3, 400 MHz) δ 7.25-7.27 (m, 2H), 6.85 (d, J=8.8 Hz, 2H), 3.80 (s, 3H), 3.62 (s, 3H), 1.58 (q, J=3.6 Hz, 2H), 1.15 (q, J=3.6 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846753B2
出典データセットuspto-grants-2014_09
ORD IDord-44b78acd95c0426cb5d8652d5eb7692a
出典メモuspto-grants-2014_09