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HRID 889236作成日:2026年10月25日

Ethyl Acetate → 2-Methanesulfonyloxy-5-methylbenzoic acid methyl ester

https://huagongshe.com/reaction/889236

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium hydrideHCID 24758—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Methyl 5-methylsalicylateHCID 89802—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methanesulfonyloxy-5-methylbenzoic acid methyl esterHCID 86638979—

反応条件

温度0 °C

反応手順

To a ice cooled suspension of sodium hydride (60%, 1.3 g, 78.3 mmol) in THF (100 mL) is added a solution of 2-hydroxy-5-methylbenzoic acid methyl ester (10 g, 60 mmol) in THF (20 mL) and it is stirred at 0° C. Then a solution of methanesulfonyl chloride (8.2 g, 72 mmol) in THF (20 mL) is added dropwise. The reaction mixture is stirred at RT for 18 h. Then the reaction mixture is cooled in an ice bath and slowly ice is added to quench the reaction. EtOAc is used to extract. Brine is added to the aqueous phase and re-extracted with EtOAc. The combined organic phase is washed with water, brine, dried over NaSO4 and MgSO4, and concentrated to give the title compound as an oil. It is used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08252820B2
出典データセットuspto-grants-2012_08
ORD IDord-bfd77a7eb4ed4c36bd2f27f4462f51ec
出典メモuspto-grants-2012_08