反応 #1267971
関連文献 (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US09206191B2
反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of 4-chloro-1-fluoro-2-nitrobenzene (9.2 g, 52.4 mmol), 4-amino-1-(4-methoxybenzyl)pyrrolidin-2-one (11.5 g, 52.4 mmol) and K2CO3 (14.5 g, 105 mmol) in 300 mL of anhydrous CH3CN was heated with stirring at 50° C. for 16 hours. The reaction mixture was filtered and the filter cake was dissolved with H2O (400 mL), and extracted with EtOAc (200 mL×4). The organic layers and the filtrate was combined and concentrated in vacuo to 50 mL. The precipitate was collected by filtration and washed with 10 mL of PE to afford 4-[(4-chloro-2-nitrophenyl)amino]-1-(4-methoxybenzyl)pyrrolidin-2-one as an orange solid (15.8 g, yield: 80.2%). was heated The reaction mixture was filtered the filter cake was dissolved with H2O (400 mL) extracted with EtOAc (200 mL×4) concentrated in vacuo to 50 mL The precipitate was collected by filtration washed with 10 mL of PE
ソース ID: ord-16a27f1b13604b4a84e05d1582a932ba