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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592718Generated: October 26, 2026

Piperazine → (s)-1-{2-[1-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-phenyl}-piperazine

https://huagongshe.com/reaction/1592718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant(5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silaneHCID 125465295—
Product(s)-1-{2-[1-(Tert-butyl-dimethyl-silanyloxy)-ethyl]-phenyl}-piperazineHCID 69410954—

Reaction Steps

To a 25 mL flask containing (S)-(−)-2-bromo-alpha-methylbenzyl alcohol (200 mg, 1.0 mmol), tert-butyldimethylsilyl chloride (165 mg, 1.1 mmol), and imidazole (203 mg, 3.0 mmol) flushed with nitrogen was added 5 mL of dimethylformamide. After stirring overnight, the mixture was quenched with saturated sodium bicarbonate, diluted with ethyl acetate, washed with NaH2PO4, saturated aqueous sodium bicarbonate, water, brine, dried (Na2SO4), filtered, and concentrated. Purification by flash chromatography (10 g SiO2, linear gradient 0-10% ethyl acetate/Hexanes, 30 mL/minute, over 30 minutes) gave about 260 mg (0.82 mmol, 82%) of (5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane as a colorless oil. GC/MS (EI): 315 (M). The (5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane was coupled to piperazine in a manner similar to Preparation 1A. LRMS (ESI+): 321.5 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291619B2
Source datasetuspto-grants-2007_11
ORD IDord-85c071762c5b43638b60d961d9083e24
Source noteuspto-grants-2007_11