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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 971092Erstellt: 24. Oktober 2026

Phosphoric Acid → (3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acid

https://huagongshe.com/de/reaction/971092

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphoric AcidHCID 1004—
EduktTriisopropyl borateHCID 21531—
EduktAmmonium ChlorideHCID 25517—
Edukttert-Butyl 4-(3-bromophenyl)piperazine-1-carboxylateHCID 10882380—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelHeptaneHCID 8900—
LösungsmittelTetrahydrofuran tolueneHCID 22635083—
Produkt(3-[4-(Tert-butoxycarbonyl)piperazin-1-YL]phenyl)boronic acidHCID 22392008—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To the 4-tert-Butyloxycarbonyl-1-(3-bromophenyl)piperazine from Step 1 (118.30 g, 346.9 mmol) in tetrahydrofuran/toluene (1/1, 1.5 L) at −78° C. under nitrogen was added n-butyllithium (2.5M, 160 mL, 398.9 mmol) dropwise and the resulting reaction mixture was stirred at −78° C. for 20 minutes. Triisopropyl borate (96.4 mL, 416.3 mmol) was added dropwise and the reaction was warmed to 0° C. and stirred for 2 hours. Aqueous saturated ammonium chloride (400 mL), water (100 mL) and 1 equivalent of H3PO4 (20 mL) were added and the mixture was stirred for 15 minutes and then concentrated to a volume of approximately 200 mL (at which stage the mixture became bluish and a precipitate formed). The mixture was slowly diluted with heptane (800 mL) and the resulting suspension was stirred overnight. The suspension was filtered, the solid was washed with heptane and dried to afford the title boronic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07312334B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-841f4d3d7ddc4b06a2cb958094345a70
Quellennotizuspto-grants-2007_12