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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856040Generated: October 30, 2026

Sodium hydride → HCID 23081564, compound

https://huagongshe.com/reaction/856040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantp-Trifluoromethylbenzyl chlorideHCID 123096—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
SolventDimethylformamideHCID 6228—
ProductHCID 23081564HCID 2308156491.6%

Reaction Steps

Sodium hydride (840 mg, 24.5 mmol) was gradually added to a solution of tert-butyl 3-oxopiperazine-1-carboxylate (4.1 g, 20.4 mmol) in DMF (30 ml) while cooling in an ice-bath, and the mixture was stirred at room temperature for 30 minutes. A solution of 4-trifluoromethylbenzyl chloride (5 g, 20.9 mmol) in DMF (5 ml) was added dropwise to the mixture while cooling in an ice-bath, which was stirred at room temperature for 2 hours. The reaction mixture was poured into ice water, and extracted with ethyl acetate twice. The extract was washed with water twice and brine, and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride) to afford tert-butyl 3-oxo-4-(4-trifluoromethylbenzyl)piperazine-1-carboxylate (6.7 g, yield 91%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-2a15bf37bbc44482ac02d6817e34bde8
Source noteuspto-grants-2007_08