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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004569Generated: October 25, 2026

Triethylamine → (+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazine

https://huagongshe.com/reaction/1004569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dimethylbenzoic acidHCID 10356—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant2-(3,4-Dichlorophenyl)piperazineHCID 4231356—
SolventDichloromethaneHCID 6344—
Product(+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazineHCID 1029215957.8%

Reaction Steps

To a cooled solution of CH2Cl2 (600 mL) containing 2-(3,4-dichlorophenyl)piperazine (6.934 g, 30 mmol), 3,5-dimethylbenzoic acid (4.55 g, 30 mmol), and N-hydroxybenzotriazole monohydrate (4.05 g, 30 mmol) at -20° C. were added Et3N (4.2 mL, 30 mmol) and N,N-dimethylaminopropylethylcarbodimide (DEC) (5.86 g, 30 mmol) under nitrogen. The reaction was kept at -20° C. for an hour and gradually warmed to RT overnight. After stirring 22 hours, the reaction was complete and CH2Cl2 (200 mL) was added. The organic solution was washed with brine (150 mL, 3×), dried over MgSO4, filtered and concentrated under vacuum to give 8.2 g of crude product. The product was crystallized from CH2Cl2 /Hexane to give a light yellow solid (6.3 g, 17.34 mmol, 57.8%). Mm.p.139-141° C.; FAB MS [M+1]+35Cl 363.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051575
Source datasetuspto-grants-2000_04
ORD IDord-f83c28f0b5ee407aa13c4f0398fad8a3
Source noteuspto-grants-2000_04