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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38299Generated: October 25, 2026

Benzyl Bromide → Tert-butyl 4-benzyl-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/38299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-benzyl-3-oxopiperazine-1-carboxylateHCID 10891590—

Reaction Steps

Sodium hydride (88 mg, 60% wt.) was added portionwise to a solution of 4-BOC-piperazinone (400 mg) in DMF (10 ml). The reaction mixture was stirred for 1 h, and then benzyl bromide (262 μl) was added dropwise and the mixture stirred at room temp for 16 h. The reaction was quenched with methanol and diluted with water, and then extracted with EtOAC. The organic extracts were concentrated in vacuo and the residue was purified by chromatography (silica, 20% ether/hexane as eluent) to give the sub-title compound (429 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524715B2
Source datasetuspto-grants-2013_09
ORD IDord-986826fa224b44c498e4e63b28714e72
Source noteuspto-grants-2013_09