戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2355006作成日:2026年10月25日

Potassium Phosphate, Tribasic → 3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/2355006

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1-Bromo-4-(methylsulphonyl)benzeneHCID 77014—
反応物2-(Di-tert-butylphosphino)biphenylHCID 2734215—
反応物Methyl 3-hydroxy-5-(methoxymethoxy)benzoateHCID 23136427—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物3-(4-Methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl esterHCID 5926331471.1%

反応条件

温度130 °C

反応手順

After adding 33.4 g (142 mmol) of 4-methanesulfonyl-bromobenzene, 2.67 g (11.9 mmol) of palladium acetate, 5.31 g (17.8 mmol) of 2-(di-tert-butylphosphino)biphenyl and 50.3 g (237 mmol) of potassium phosphate to a solution of 25.0 g (119 mmol) of 5-hydroxy-3-methoxymethoxybenzoic acid methyl ester in toluene (375 ml), the reactor was sealed and the mixture was subsequently stirred at 130° C. for 6 hours. Acetic acid ethyl ester was added to the reaction mixture, which was then filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:acetic acid ethyl ester=2:1) to obtain 31.0 g of 3-(4-methanesulfonyl-phenoxy)-5-methoxymethoxy-benzoic acid methyl ester (yield: 69%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07754743B2
出典データセットuspto-grants-2010_07
ORD IDord-8dbd8fa8486c47e6a4f2277da2e4f1a7
出典メモuspto-grants-2010_07