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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176914Generated: November 1, 2026

Acetic Acid → (Z)-ethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)but-2-enoate

https://huagongshe.com/reaction/2176914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl cyanoacetateHCID 7764—
Reactant4-(4-Methyl-1-piperazinyl)acetophenoneHCID 33551—
ReactantAmmonium AcetateHCID 517165—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product(Z)-ethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)but-2-enoateHCID 8665755732.4%

Reaction Conditions

Temperature137.5 °C

Reaction Steps

Ethyl cyano acetate (3.12 g, 27.6 mmol), ammonium acetate (123 mg, 1.76 mmol), acetic acid (0.2 ml, 3.5 mmol) were added successively to a stirred solution of 1-(4-(4-methylpiperazin-1-yl)phenyl)ethanone (5.0 g, 23 mmol) in benzene (25 ml) and stirred for 36 h at 135-140° C. The reaction mixture was poured into water and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. This was purified by column chromatography using 2% methanol in CHCl3 as eluent to afford (Z)-ethyl 2-cyano-3-(4-(4-methylpiperazin-1-yl)phenyl)but-2-enoate as yellow liquid 2.30 g (32.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067888B2
Source datasetuspto-grants-2015_06
ORD IDord-d55d6f5570954d8ea54cf21a1171517d
Source noteuspto-grants-2015_06