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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416651Generated: October 25, 2026

Diisopropylethylamine → tert-Butyl 4-(3,3,3-trifluoropropyl)-1-piperazine-carboxylate

https://huagongshe.com/reaction/2416651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-1,1,1-trifluoropropaneHCID 2725114—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(3,3,3-trifluoropropyl)-1-piperazine-carboxylateHCID 22633053—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)piperazine (5.00 g) and N,N-diisopropylethylamine (4.68 ml) in N,N-dimethylformamide (13 ml) was added 1-bromo-3,3,3-trifluoropropane (5.00 ml) at 60° C. The mixture was stirred at 60° C. for 4 hours. The reaction mixture was poured into saturated aqueous sodium hydrogencarbonate solution and extracted with hexane. The organic layer was washed successively with saturated aqueous ammonium chloride solution, aqueous sodium hydrogencarbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated to give the title compound (5.38 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825200B1
Source datasetuspto-grants-2004_11
ORD IDord-facdc45277a04f8898a6d24147b75bce
Source noteuspto-grants-2004_11