125971-57-5

基本信息
2-亞芐基-N-苯基-異丁基乙酰胺
2-BENZYLIDENE-N-PHENYL-ISOBUTYLOYLACETAMIDE
4-METHYL-3-OXO-N-PHENYL-2-(PHENYLMETHYLENE)PENTANAMIDE
2-Benylidine isobutyryl acetanilide
4-METHYL-3-OXO-N-PHENYL-2-(PHENYLMETHYLENE)-PENTAN
2-Isobutyryl-N-phenyl-3-phenylacrylamide
物理化學(xué)性質(zhì)
制備方法

124401-38-3

100-52-7

125971-57-5
在氮氣保護下,向裝有溫度計和1000 mL機械攪拌器的反應(yīng)燒瓶中,加入第二中間體2-甲基-3,5-二羰基-5-苯胺基丁烷41 g(0.2 mol)和250 mL正庚烷。加熱回流以除去生成的水,反應(yīng)持續(xù)約6小時。反應(yīng)體系冷卻至室溫后,依次加入催化劑甘氨酸4 g和冰醋酸6 g,隨后加入苯甲醛24 g(0.22 mol)。將反應(yīng)混合物加熱至回流溫度,繼續(xù)反應(yīng)約8小時,期間通過TLC監(jiān)測反應(yīng)進程。反應(yīng)完成后,冷卻至室溫,用50 mL飽和氯化鈉溶液洗滌反應(yīng)混合物。加入100 mL正庚烷后,分離有機相,并用無水硫酸鈉干燥。減壓濃縮濾液,得到目標(biāo)產(chǎn)物4-甲基-3-氧代-N-苯-2-(亞芐基)戊酰胺46 g。
參考文獻:
[1] Organic and Biomolecular Chemistry, 2016, vol. 14, # 7, p. 2291 - 2296
[2] Tetrahedron Letters, 1992, vol. 33, # 17, p. 2283 - 2284
[3] RSC Advances, 2014, vol. 4, # 63, p. 33175 - 33183
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 2000, vol. 43, # 3, p. 261 - 270
[5] Journal of the Indian Chemical Society, 2010, vol. 87, # 4, p. 495 - 499