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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375019Generated: October 31, 2026

Water → 1-Acetyl-3-[[3-methoxy-4-(trifluoromethyl)phenyl]methylene]piperazine-2,5-dione

https://huagongshe.com/reaction/1375019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-Diacetyl-2,5-piperazinedioneHCID 540371—
Reactant3-Methoxy-4-(trifluoromethyl)benzaldehydeHCID 17964170—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product1-Acetyl-3-[[3-methoxy-4-(trifluoromethyl)phenyl]methylene]piperazine-2,5-dioneHCID 69420099—

Reaction Steps

To a stirred mixture of crude 3-methoxy-4-(trifluoromethyl)-benzaldehyde and 1,4-diacetylpiperazine-2,5-dione (1.98 g) in a mixture of N,N-dimethylformamide (10 ml) and tert-butanol (10 ml) was added potassium tert-butoxide (1.12 g) at 5° C. The mixture was stirred for 18 hours at room temperature. Water (30 ml) and ethyl acetate (100 ml) were added to the mixture and the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The combined extract was washed with water, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel with 50% of ethyl acetate in hexane as an eluent to give 1-acetyl-3-[[3-methoxy-4-(trifluoromethyl)phenyl]methylene]piperazine-2,5-dione (2.11 g) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166598B2
Source datasetuspto-grants-2007_01
ORD IDord-f49e23d9496549a4970675962c087491
Source noteuspto-grants-2007_01