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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354587Generated: October 31, 2026

Triethylamine → HCID 57430050, compound

https://huagongshe.com/reaction/2354587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Phenylpropionic acidHCID 10296—
ReactantThionyl ChlorideHCID 24386—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
CatalystDimethylformamideHCID 6228—
Solvent1,2-DichloroethaneHCID 11—
SolventDiethyl EtherHCID 3283—
ProductHCID 57430050HCID 57430050—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of 2-phenyl propionic acid (1.0 g, 6.7 mmol) in 1,2-dichloroethane (15 mL) was added a few drops of DMF and excess thionyl chloride. The resulting mixture was heated at reflux for 2 h, when bubbling ceased the mixture was evaporated to dryness. The crude residue was co-evaporated with toluene and 1,2-dichloroethane. The residue was dissolved in CH2Cl2 and cooled to 0° C. To the stirred solution, BOC-piperazine (1.24 g, 6.7 mmol) and Et3N were added. A white precipitate formed and the reaction was stirred 12 h at RT. Et2O was added and the mixture was washed with water and brine. The ether layer was separated and dried over anhydrous Na2SO4, filtered, and evaporated. The residue was treated with 20% ether/hexanes and the resulting solid filtered. The filtrate was evaporated and the procedure repeated. After drying, there remained a white solid (1.3 g, 62%). 1H NMR (CDCl3) δ: 1.4 (s, 9H), 1.42 (d, 3H), 2.7 (m, 1H), 3.1-3.6 (m, 6H), 3.85 (m, 2H), 7.2-7.4 (m, 5H). [M+Na] 341.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754724B2
Source datasetuspto-grants-2010_07
ORD IDord-43b63ad9d9a641028f99f47f6a56a9bf
Source noteuspto-grants-2010_07