戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 987937作成日:2026年10月26日

Sodium hydride → 2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylsulfanyl)-propionic Acid Methyl Ester

https://huagongshe.com/reaction/987937

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-FluorothiophenolHCID 67789—
反応物2-Tert-butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl esterHCID 2818162—
溶媒DimethylformamideHCID 6228—
生成物2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylsulfanyl)-propionic Acid Methyl EsterHCID 69853553—

反応手順

A stirred solution of 4-fluorothiophenol (1.24 g, 9.65 mmol) in N,N-dimethyl formamide (10 ml) was treated with sodium hydride (240 mg, 9.37 mmol) and the reaction mixture was stirred at room temperature for 30 minutes. 2-tert-Butoxycarbonylamino-3-(toluene-4-sulfonyloxy)-propionic acid methyl ester (3 g, 8.04 mmol) in N,N dimethyl formamide (ml) was added, the resulting mixture was stirred for two hours and then concentrated in vacuo. The residue was dissolved in ethyl acetate (100 ml) and washed with water (2*80 ml) and brine. The organic layer was dried (anhydrous magnesium sulfate) and concentrated in vacuo to give, after purification by flash chromatography on silica gel, 2-tert-butoxycarbonylamino-3-(4-fluoro-phenylsulfanyl)-propionic acid methyl ester (2.28 g, 83%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06632826B1
出典データセットuspto-grants-2003_10
ORD IDord-b64c81fbdb9f4444baef37d83817bdde
出典メモuspto-grants-2003_10