反应 #1256762

ord-618bf7a24ccb4877b66cc7b85a5d3f06

反应方程式

CC(=O)[O-].[NH4+]
ammonium acetate
CCOC(=O)CC#N
ethyl cyanoacetate
CCOC(=O)C1(C(C)=O)CC1
1-acetyl-cyclopropanecarboxylic acid ethyl ester
O=Cc1ccc([N+](=O)[O-])cc1
4-nitrobenzaldehyde
CCOC(=O)C1(c2cc(-c3ccc([N+](=O)[O-])cc3)c(C#N)c(=O)[nH]2)CC1
product
收率 43.4%
CCOC(=O)C1(c2cc(-c3ccc([N+](=O)[O-])cc3)c(C#N)c(=O)[nH]2)CC1
1-[5-Cyano-4-(4-nitro-phenyl)-6-oxo-1,6-dihydro-pyridin-2-yl]-cyclo-propanecarboxylic acid ethyl ester
收率 43.4%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

In analogy to GP 1, reaction of 28.9 g ammonium acetate (375 mmol, 8 eq.), 5 ml ethyl cyanoacetate (47.3 mmol, 1 eq.), 7.32 g 1-acetyl-cyclopropanecarboxylic acid ethyl ester (47 mmol, 1 eq.), and 7.08 g 4-nitrobenzaldehyde (47 mmol, 1 eq.) yielded 7.2 g product (43% yield).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07825114B2uspto-grants-2010_11