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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109832Generated: October 31, 2026

Diethyl Oxalate → HCID 54684774, compound

https://huagongshe.com/reaction/2109832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-Acetyl-2-piperazinoneHCID 12744517—
SolventDimethylformamideHCID 6228—
ProductHCID 54684774HCID 54684774—

Reaction Steps

To a cold (0° C.) solution of 4-acetylpiperazin-2-one (1.0 g, 7.0 mmol) in DMF (75 mL) under an atmosphere of nitrogen, a solution of lithium bis(trimethylsilyl)-amide in THF (7.7 mL, 7.7 mmol) was added and stirred at the temperature for 30 min. The resultant solution was treated with 3-chlorobenzyl bromide (0.92 mL, 7.0 mmol), and stirred at room temperature overnight. The resultant mixture was cooled to 0° C., treated with a solution of lithium bis(trimethylsilyl)amide in THF (8.4 mL, 8.4 mmol) and stirred for 30 min, and then treated with diethyl oxalate (0.96 mL, 7.0 mmol). The resultant mixture was stirred at room temperature overnight. Additional solution of lithium bis(trimethylsilyl)amide in THF (16.8 mL, 16.8 mmol) was added and stirred for 4 hrs. The product mixture was concentrated under vacuum, and the residue was treated with a mixture of aqueous HCl and ethyl acetate. The white solid precipitated was collected by filtration and was subjected to HPLC purification on C-18 stationary phase eluted with water/acetonitrile/TFA mobile phase. Collection and lyophilization of appropriate fractions provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517532B2
Source datasetuspto-grants-2009_04
ORD IDord-c9e79b274c7f4a32a66f9ba2365b86b2
Source noteuspto-grants-2009_04