Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737143Generated: November 3, 2026

Ethyl Bromide → HCID 57849476, compound

https://huagongshe.com/reaction/737143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57849460HCID 57849460—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57849476HCID 57849476—

Reaction Steps

This compound was made in the following manner: 100 mg of 3-(S)-benzyl-1-(2′-chloro-biphenyl-4-ylmethyl)-piperazine was dissolved in THF, 3 equiv. of N,N-diisopropylethylamine were added followed by 2 equiv. of bromoethane. The reaction was be shaken at room temperature overnight. The reaction was concentrated in vacuo. The residue was diluted with DCM and washed with 1N aqueous NaOH solution. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified by column chromatography to afford the title compound as free base. Treatment with 1 equiv. 2M HCl in dioxane and concentration in vacuo gave 16 mg of its hydrochloride salt. Yield 27%, ES MS (+) m/z 405

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-671af99aaa0a42099b93c99e1ebcff39
Source noteuspto-grants-2009_09