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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1739693Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1739693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3,5-Dimethylbenzoic acidHCID 10356—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt2-(3,4-Dichlorophenyl)piperazineHCID 4231356—
LösungsmittelDichloromethaneHCID 6344—
Produkt(+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazineHCID 1029215957,8%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05968929
Quelldatensatzuspto-grants-1999_10
ORD IDord-56f244677fc849b4926270e5ea779790
Quellennotizuspto-grants-1999_10