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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798354Generated: November 4, 2026

Water → 4-[2,2-Bis-(4-chloro-phenyl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1798354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBis(4-chlorophenyl)acetaldehydeHCID 167694—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product4-[2,2-Bis-(4-chloro-phenyl)-ethyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 5933195211.1%

Reaction Steps

To a solution of bis-(4-chloro-phenyl)-acetaldehyde (3.74 mmol) in methanol under a nitrogen atmosphere, N-BOC-piperazine (1.05 g, 5.61 mmol) was added, the reaction mixture was stirred for 1 hour before addition of sodium cyanoborohydride (0.28 g, 4.49 mmol). The reaction mixture was stirred for 18 hours, water added (3 ml) and the solvent removed under reduced pressure. The residue was partitioned between dichloromethane and water, the organic layer was separated, dried (MgSO4), filtered and concentrated. Purified over flash silica chromatography eluting with ethyl acetate/petroleum ether (3:7) to yield the title compound (0.18 g, 11% yield for steps 30A and 30B combined). LC/MS: (PS-A2) Rt 2.66 [M-BOC+H]+335.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343953B2
Source datasetuspto-grants-2013_01
ORD IDord-a6fce814d9af43e7b313a274af2fd718
Source noteuspto-grants-2013_01