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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534918Generated: October 31, 2026

Triethylamine → 3-(4-(2-Tert-butylphenyl)piperazin-1-yl)-3-oxopropanenitrile

https://huagongshe.com/reaction/534918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyanoacetic acidHCID 9740—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Reactant1-(2-Tert-butylphenyl)piperazineHCID 46941659—
SolventDichloromethaneHCID 6344—
Product3-(4-(2-Tert-butylphenyl)piperazin-1-yl)-3-oxopropanenitrileHCID 6675116358%

Reaction Steps

To a stirred solution of provide 1-(2-tert-butylphenyl)piperazine (0.203 g, 0.69 mmol), 2-cyanoacetic acid (0.065 g, 0.77 mmol) and triethylamine (0.279 g, 2.76 mmol) in methylene chloride (5.0 mL) was added bis(2-oxo-3-oxazolidinyl)phosphinic chloride (0.202 g, 0.77 mmol) at room temperature. After 2.5 h the reaction mixture was diluted with methylene chloride (10.0 mL), washed with water (20.0 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, 50% ethyl acetate/heptanes) to provide 3-(4-(2-tert-butylphenyl)piperazin-1-yl)-3-oxopropanenitrile (0.114 g, 58%) as an off-white solid, mp 163-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-5edb6740382d493e85b3f95285e25da9
Source noteuspto-grants-2014_10