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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944859Generated: October 31, 2026

Benzyl piperazine-1-carboxylate → Benzyl 4-(6-((tert-butyldimethylsily)oxy)hexyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1944859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
Reactant(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
SolventAcetonitrileHCID 6342—
ProductBenzyl 4-(6-((tert-butyldimethylsily)oxy)hexyl)piperazine-1-carboxylateHCID 5850509270%

Reaction Steps

Intermediate 19 (2.6 g, 8.8 mmol) was added to a stirring solution of benzyl piperazine-1-carboxylate (1.1 mL, 5.87 mmol) in CH3CN (80 mL). The reaction mixture was refluxed over night, cooled, and quenched with satd. NaHCO3 (100 mL). The aqueous layer was extracted with EtOAc (3×50 mL) and the combined organic layers were washed with brine, dried over Na2SO4, concentrated to give the crude (3.8 g) as opaque oil. The chromatography (1:3, hexanes/EtOAc) afforded the title compound (1.78 g, 70%) as clear oil. ES/MS calcd. for C24H43N2O3Si+ 435.3. Found m/z=435.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394829B2
Source datasetuspto-grants-2013_03
ORD IDord-b7517b6ce9024bc09510a8896555697d
Source noteuspto-grants-2013_03