Skip to main content
. 2023 Aug 21;13(35):24846–24853. doi: 10.1039/d3ra04590k

GT reaction of ethyl cyanoacetate, (NH4)2CO3, and 1,3-dicarbonylsa.

graphic file with name d3ra04590k-u2.jpg
Entry R R1 Product Time (h) Isolated yield (%)
1 CH3 OEt graphic file with name d3ra04590k-u3.jpg 4 96
2 CH3 OMe graphic file with name d3ra04590k-u4.jpg 3.5 98
3 CH3 O-tBu graphic file with name d3ra04590k-u5.jpg 8 85
4 Ph OEt graphic file with name d3ra04590k-u6.jpg 7 93
5 CF3 OEt graphic file with name d3ra04590k-u7.jpg 2.5 95
6 CH2Cl OEt graphic file with name d3ra04590k-u8.jpg 9 90
7 n-Propyl OEt graphic file with name d3ra04590k-u9.jpg 7 85
8 Me Me graphic file with name d3ra04590k-u10.jpg 5 90
9 Me Ph graphic file with name d3ra04590k-u11.jpg 4 87
10 CF3 graphic file with name d3ra04590k-u12.jpg graphic file with name d3ra04590k-u13.jpg 4 84
11 CF3 Me graphic file with name d3ra04590k-u14.jpg 3 90
a

Reaction conditions: ethyl cyanoacetate (1 mmol), 1,3-dicarbonyl (1 mmol), (NH4)2CO3 (2 mmol), H2O : EtOH (1 : 1), 80 °C.