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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190227Generated: November 1, 2026

N-bromobutanimide → HCID 58994541, compound

https://huagongshe.com/reaction/1190227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 58994384HCID 58994384—
SolventAcetonitrileHCID 6342—
ProductHCID 58994541HCID 5899454132%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-{4-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-piperazin-1-ylmethyl}-phenylamine (as prepared in the previous step, 204 mg, 0.582 mmol) in CH3CN (6 mL) was cooled to 0° C. and treated dropwise with NBS as a solution in CH3CN (6 mL). The solvents were evaporated in vacuo. The residue was taken up in EtOAc and washed with satd aq NaHCO3. The organic layer was dried over MgSO4 and concentrated in vacuo. Purification of the residue on a 20-g Isolute SPE column on a FlashMaster system with 25-50% EtOAc-hexane afforded the title compound (80.9 mg, 32%) as an off-white solid. Mass spectrum (ESI, m/z): Calcd. for C19H34N3OSiBr, 428.2/430.2 (M+H). found 428.1/430.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674100B2
Source datasetuspto-grants-2014_03
ORD IDord-5a6e831f19cd45129c3d25d09f1c0b28
Source noteuspto-grants-2014_03