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HRID 417988Erstellt: 25. Oktober 2026

Diisopropylethylamine → 3-Bromo-1-(4-chlorophenyl)piperazine 2,2-dimethylpropan-1-one

https://huagongshe.com/reaction/417988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3-Bromo-2,2-dimethylpropanoic acidHCID 271932—
EduktPiperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2)HCID 12212341—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelThionyl ChlorideHCID 24386—
Produkt3-Bromo-1-(4-chlorophenyl)piperazine 2,2-dimethylpropan-1-oneHCID 8663577629,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-Bromo-2,2-dimethylpropionic acid (1.50 g, 8.29 mmol) was dissolved in thionyl chloride (10 mL) and DMF (0.1 mL). The reaction mixture was heated at reflux for 1.5 hours and then concentrated in vacuo, The residue was dissolved in DCM (10 mL) and added to a solution of 4-chlorophenyl piperazine dihydrochloride (2.35 g, 8.70 mmol) and DIPEA (5.05 mL, 29.0 mmol) in DCM (20 mL) at 0° C. The reaction mixture was stirred at 0° C. for 2 hours and then concentrated in vacuo. The residue was dissolved in DCM (100 mL) and washed with 10% citric acid solution (50 mL), sat aq NaHCO3 solution (50 mL), brine (50 mL), dried (MgSO4) and concentrated in vacuo. The resulting residue was purified using normal phase column chromatography (eluting with heptane, followed by a 1:1 mixture of EtOAc:heptane) to give 3-bromo-1-(4-chlorophenyl)piperazine-2,2-dimethyl-propan-1-one (0.87 g, 29.3%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093248B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-1ddbff1a4f0c4fd78f75d394fac43362
Quellennotizuspto-grants-2012_01