戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1961452作成日:2026年10月27日

N,N-Diethyl-2,2,2-trifluoroacetamide → HCID 68071560、化合物

https://huagongshe.com/reaction/1961452

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-Diethyl-2,2,2-trifluoroacetamideHCID 225443—
反応物tert-butyl N-(1-(4-bromophenyl)ethyl)carbamateHCID 11983730—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 68071560HCID 6807156046%

反応条件

温度-78 °C

反応手順

tert-Butyl 1-(4-bromophenyl)ethylcarbamate (6.35 g, 21.2 mmol) was dissolved in dry THF (100 ml) and cooled to −78° C. under an atmosphere of nitrogen. n-Butyllithium (21 ml, 52.9 mmol, 2.5M in hexanes) was added dropwise under 10 minutes and the reaction was stirred at −78° C. for 3 hours. A solution of diethyl trifluoroacetamide (5.0 g, 29.6 mmol) in 10 ml dry THF was added dropwise and the reaction was stirred 1.5 hours at −78° C. Reaction was quenched with NH4Cl (sat) (50 ml) and H2O (50 ml) and allowed to reach room temperature. The aqueous phase was separated and extracted with EtOAc (100 ml). The combined organics were washed with NH4Cl (sat) (2*100 ml), H2O (100 ml), dried over MgSO4, filtered and evaporated. Unreacted starting material was removed by precipitation from MeOH/H2O (9/1). The mother liquor was evaporated and the residue purified by flash chromatography using Pet. Ether/EtOAc (7:1→5:1) as eluent to give 3.09 g (46%) of the title compound as white solids.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08415333B2
出典データセットuspto-grants-2013_04
ORD IDord-496dc8c8d91a4722ba9767de7dd1ea91
出典メモuspto-grants-2013_04