Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634229Generated: October 31, 2026

Ethyl 2-methylacetoacetate → 2-(2-Cyano-3-methylamino-4-nitrophenyl)-2-methyl-3-oxobutyric acid ethyl ester

https://huagongshe.com/reaction/1634229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Chloro-2-(methylamino)-3-nitrobenzonitrileHCID 11218089—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product2-(2-Cyano-3-methylamino-4-nitrophenyl)-2-methyl-3-oxobutyric acid ethyl esterHCID 1203547160%

Reaction Steps

To a stirred solution of potassium t-butoxide (24.3 g, 206 mmol) in DMSO (500 mL) was added ethyl 2-methylacetoacetate (34.3 g, 233 mmol), dropwise over 5 min. The temperature rose to 30° C. 6-Chloro-2-methylamino-3-nitrobenzonitrile (43.6 g, 190 mmol) was added in portions over 15 min. The temperature rose to 40° C. The solution was stirred for 1 h with no external heating or cooling. The mixture was poured into 10% NH4Cl (500 mL), and extracted with EtOAc (2×500 mL). The combined extracts were washed with water (2×250 mL) and brine, and evaporated. MeOH (200 mL) was added to the residue and stirred for 1.5 h. The yellow solid was filtered, washed with cold MeOH (25 mL) and dried to give 2-(2-cyano-3-methylamino-4-nitrophenyl)-2-methyl-3-oxobutyric acid ethyl ester (36.2 g, 60%), mp 87-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506769B2
Source datasetuspto-grants-2003_01
ORD IDord-bbb232a36da24fa88955e92f8c0eb043
Source noteuspto-grants-2003_01