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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 417990Erstellt: 25. Oktober 2026

Oxalyl chloride → 3-Bromo-1-(4-methylphenyl)piperazine 2,2-dimethylpropan-1-one

https://huagongshe.com/reaction/417990

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
EduktDiisopropylethylamineHCID 81531—
Edukt1-(p-Tolyl)piperazine dihydrochlorideHCID 83112—
Edukt3-Bromo-2,2-dimethylpropanoic acidHCID 271932—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-1-(4-methylphenyl)piperazine 2,2-dimethylpropan-1-oneHCID 8663577852%

Reaktionsschritte

3-Bromo-2,2-dimethylpropionic acid (10.0 g, 55.3 mmol) was dissolved in DCM (60 mL). Oxalyl chloride (7.20 mL, 82.9 mmol) was added slowly over 10 minutes. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was dissolved in DCM (40 mL) and added to a solution of 4-methylphenyl-piperazine dihydrochloride (13.76 g, 55.3 mmol) and DIPEA (33.0 mL, 193.4 mmol) in DCM (100 mL) at 0° C. The reaction mixture was allowed to warm to room temperature over 1 hour and then stirred at room temperature for 16 hours. The reaction mixture was washed with 10% citric acid solution (2×100 mL), dried (MgSO4) and concentrated in vacuo to give 3-bromo-1-(4-methylphenyl)piperazine-2,2-dimethylpropan-1-one (9.62 g, 52%) as a white solid which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093248B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-43dd9f090fc14470b0593744eb01787f
Quellennotizuspto-grants-2012_01