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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978382Generated: October 29, 2026

Benzyl Bromide → HCID 70246716, compound

https://huagongshe.com/reaction/1978382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
Reactant(2S,5R)-1-Boc-2,5-dimethylpiperazineHCID 11745988—
SolventAcetonitrileHCID 6342—
ProductHCID 70246716HCID 70246716—

Reaction Steps

To an acetonitrile (40 ml) solution of 4.5 g (21.0 mmol.) of trans-1-tert-butoxycarbonyl-2,5-dimethyl piperazine and 5.9 ml (42.3 mmol.) of triethylamine was added, at room temperature, 3.2 ml (26.9 mmol.) of benzyl bromide. The mixture was heated for 24 hours under reflux. The solvent was distilled off under reduced pressure. To the residue was added water. The mixture was subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous saline solution, which was dried over magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by means of a column chromatography (ethyl acetate/hexane 10%) to give the object compound as a pale yellow oily product. The yield was 5.17 g (81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-6c3773c9bc4147aa8332e686254d96b6
Source noteuspto-grants-2001_05