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HRID 887667作成日:2026年10月25日

Trifluoroacetic anhydride → 2,2,2-Trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamide

https://huagongshe.com/reaction/887667

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic anhydrideHCID 9845—
反応物DiisopropylethylamineHCID 81531—
反応物Benzeneethanamine, 4-nitro-, hydrochloride (1:1)HCID 458983—
溶媒DichloromethaneHCID 6344—
生成物2,2,2-Trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamideHCID 6423744—

反応手順

To a solution of 4-nitrophenethylamine hydrochloride (50 g, 0.247 mole), DIEA (128 mL, 0.74 mole, 3 eq.) and CH2Cl2 (500 mL) in a 1 L round bottom flask equipped with a magnetic stirrer was added (CF3CO)2O (52.5 mL, 0.37 mole, 1.5 eq) dropwise at 5-10° C. (with ice/water bath). After stirring for another 1 h after the addition at RT, the reaction was quenched with water (200 mL) and transferred into a separatory funnel. The organic layer was separated, washed with water and sat. NH4Cl, dried over Na2SO4, filtered, concentrated to give a brown oil. The crude was triturated with water (300 mL), filtered and dried on vacuum overnight to give the desired 2,2,2-trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamide as a yellow solid. This can be used for next step without further purification. An analytical sample was obtained through recrystallization from CH3OH/H2O as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08247430B2
出典データセットuspto-grants-2012_08
ORD IDord-b1f2ea9aff9a4066930400f85f987c56
出典メモuspto-grants-2012_08