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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484136Generated: October 29, 2026

Bromide ion → HCID 14856171, compound

https://huagongshe.com/reaction/484136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
ReactantSodium IodideHCID 5238—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14856127HCID 14856127—
SolventAcetonitrileHCID 6342—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 14856171HCID 14856171—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 3-(4-bromobutyl)-5-phenyl-4-thiazolidinone (4.67 g), 1-(3-trifluoromethylphenyl)piperazine (3.76 g), K2CO3 (5.15 g), NaI (300 mg) and CH3CN (150 mL) was heated at reflux (bath temperature 95° C.) under N2. After 17 hours, TLC analysis (silica gel, 5% MeOH/EtOAc) showed the absence of starting bromide and presence of one major product with an Rf =0.33. The mixture was cooled to room temperature, EtOAc (100 mL) was added, and the mixture filtered. The filtrate was concentrated in vacuo to an oil which was triturated with EtOAc. The mixture was filtered and the filtrate concentrated again in vacuo to 7.59 g of an oil. The crude product was chromatographed (Waters Prep 500, 2 columns, silica gel, 5% MeOH/EtOAc) to give 6.42 g of an oil, and from this 4.47 g of the oxalate salt of this amine was prepared. The solid was recrystallized from EtOH/EtOAc giving 3.65 g of fine white crystals, mp 140°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229388
Source datasetuspto-grants-1993_07
ORD IDord-a025b4283c0045faacd13aa8ee08711e
Source noteuspto-grants-1993_07