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HRID 72238作成日:2026年10月25日

Diisopropylamine → 5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/72238

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物1-PiperidinecarboxaldehydeHCID 17429—
反応物Ammonium ChlorideHCID 25517—
反応物Methyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 2805185—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl esterHCID 57618725—

反応条件

温度0 °C

反応手順

A 1.6M n-BuLi solution in hexane (12 mL) was added dropwise to a solution of diisopropylamine (2.9 mL) in THF (30 mL) at −78° C. The reaction mixture was stirred at 0° C. for 10 min and then cooled to −78° C., and a solution of 3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester (1.5 g) in THF (15 mL) was added. The reaction mixture was stirred at −78° C. for 30 min and then 1-formylpiperidine (4 g) was added, and the mixture was again stirred at this temperature for 1.5 h. Subsequently, saturated ammonium chloride solution was added and the reaction mixture was allowed to reach room temperature. The aqueous phase was extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulfate and the solvent was removed in vacuo. The product with the molecular weight of 281.0 (C9H6F3NO4S) was obtained in this way; MS (ESI): 282 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828991B2
出典データセットuspto-grants-2014_09
ORD IDord-063af6f49cc04f6fbaaa08dfff6a4a13
出典メモuspto-grants-2014_09