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. 2020 Jul 17;10(45):26771–26776. doi: 10.1039/d0ra02757j

Substrate scope of CsNF-catalyzed Knoevenagel condensationa.

graphic file with name d0ra02757j-u2.jpg
Entry 2 Product % Yieldb (3/4)
CsNF n-Hexylamine
1 graphic file with name d0ra02757j-u3.jpg 3b 76/n.dc 10/81
2 graphic file with name d0ra02757j-u4.jpg 3c 86/n.dc n.dc/91
3d graphic file with name d0ra02757j-u5.jpg 3d 53/n.dc n.dc/87
4 graphic file with name d0ra02757j-u6.jpg 3e 75/2 11/79
5 graphic file with name d0ra02757j-u7.jpg 3f 76/2 5/86
6 graphic file with name d0ra02757j-u8.jpg 3g 79/2 1/91
a

Unless otherwise noted, the reaction was carried out using 1 (2.0 mmol, 203.3 μL) and 2 (1.0 mmol, 106.2 μL) in MeOH (22.5 mL)/H2O (7.5 mL).

b

Determined by 1H NMR analysis using CH2Br2 as an internal standard.

c

Not detected.

d

The reaction was carried out for 24 h.