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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942406Generated: November 2, 2026

Triethylamine → 5-Oxo-5-(4-phenylpiperazin-1-yl)pentanal

https://huagongshe.com/reaction/1942406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Hydroxy-1-(4-phenylpiperazin-1-yl)pentan-1-oneHCID 66937601—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product5-Oxo-5-(4-phenylpiperazin-1-yl)pentanalHCID 86651315—

Reaction Steps

A solution of 1.11 mL (12.8 mmol) oxalyl chloride in 35 mL of dichloromethane is cooled to −80° C. under argon atmosphere. 2.33 mL (32.7 mmol) of dimethylsulfoxide in 9.33 mL of dichloromethane is introduced dropwise over 10 minutes. After 5 minutes a solution of 1.84 (7 mmol) 5-hydroxy-1-(4-phenylpiperazin-1-yl)pentan-1-one in 8 mL dichloromethane and 2 mL dimethylsulfoxide is added over the course of 10 minutes. The reaction mixture is stirred for another hour at −80° C. before 5 mL of triethylamine is added and the mixture is allowed to warm up to room temperature. 50 mL of saturated brine solution is added for hydrolysis. The organic phase is separated, extracted three times with a saturated solution of sodium chloride, dried over sodium sulfate and the solvent is evaporated. The crude product is obtained in almost quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389555B2
Source datasetuspto-grants-2013_03
ORD IDord-d48f935d23634ba298dd4290c79c7b38
Source noteuspto-grants-2013_03