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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 447330Erstellt: 24. Oktober 2026

Acetic Acid → 1-(4-Bromophenyl)-4-isopropylpiperazine

https://huagongshe.com/de/reaction/447330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcetoneHCID 180—
Edukt1-(4-Bromophenyl)piperazineHCID 2735629—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelDce thfHCID 21493386—
Produkt1-(4-Bromophenyl)-4-isopropylpiperazineHCID 1140333199%

Reaktionsschritte

To a mixture of 1-(4-bromophenyl)piperazine (1.20 g, 5 mmol) and acetone (1.47 mL, 20 mmol) in DCE/THF (45 mL/15 mL) was added NaBH(OAc)3 (1.38 g, 6.5 mmol), followed by AcOH (0.5 mL). After addition, the resulting mixture was stirred O/N at rt. The reaction as quenched with NaHCO3 (10 mL) and H2O (10 mL), and was extracted with EtOAc (60 mL×2). The solvents were removed in vacuo to give the crude title compound as a white solid (1.40 g, 99%). 1H NMR (400 MHz, DMSO-d6) δ 7.45 (d, J=7.2 Hz, 2H), 7.21 (d, J=7.2 Hz, 2H), 3.64-3.55 (m, 2H), 3.44 (s, 2H), 2.68 (d, J=11.6 Hz, 2H), 1.75 (t, J=11.0 Hz, 2H), 1.54 (d, J=6.0 Hz, 6H); MS ESI 282.9 [M+H]+, calcd. for [C13H19BrN2+H]+ 283.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481533B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-ffc87ca68d7a4e6e964702f194c2eccc
Quellennotizuspto-grants-2013_07