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HRID 1439作成日:2026年10月25日

Ethyl Acetate → N-t-butyl-3-chloroacetyl-2-thiophenesulfonamide

https://huagongshe.com/reaction/1439

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Ammonium ChlorideHCID 25517—
反応物3-bromo-N-tert-butylthiophene-2-sulfonamideHCID 14051925—
反応物ButyllithiumHCID 178418339—
生成物N-t-butyl-3-chloroacetyl-2-thiophenesulfonamideHCID 1969076669%

反応条件

温度-78 °C

反応手順

2.98 g (0.0| mole) of N-t-butyl-3-bromo-2-thiophenesulfonamide was dissolved in 50 ml of dry tetrahydrofura mixture was cooled to -78° C. under nitrogen gas. To the reaction solution was slowly added dropwise 8.4 ml of n-butyl lithium(2.5N) and then the temperature of the mixture was raised slowly to -20° C. and again cooled to -78° C. 1.4 g (0.012 mole) of ethyl chloroacetates was added slowly to the mixture. The temperature of the reaction mixture was raised slowly to -20° C. again and then the mixture was stirred for 10 minutes. To the mixture was added 100 ml of aqueous ammonium chloride solution and then added 100 ml of ethyl acetate to separate the organic layer. The extracted organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to column chromatography on silica gel to obtain 1.9 g (Yield: 69%) of the pure title compound as a liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726127
出典データセットuspto-grants-1998_03
ORD IDord-5c044a04ef604d88b3d7ec14794c7e4f
出典メモuspto-grants-1998_03