Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 646Erstellt: 27. Oktober 2026

tert-Butyl piperazine-1-carboxylate → HCID 130471524, Verbindung

https://huagongshe.com/reaction/646

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktMethyl 3-bromo-5-fluorobenzoateHCID 21942598—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 130471524HCID 13047152471,85%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To methyl 3-bromo-5-fluorobenzoate (1.5 g, 6.44 mmol) dissolved in dry THF (20 mL) was added tert-butyl piperazine-1-carboxylate (1.199 g, 6.44 mmol), Sodium-t-butoxide (1.856 g, 19.31 mmol) and purged with N2 gas for 10 min followed by the addition of2-(Dicyclohexylphosphino)-2',4',6'-tri-i- propyl-1,1'-biphenyl (0.307 g, 0.64 mmol), Palladium II acetate (0.145 g, 0.64 mmol) . The contents were further purged with N2 gas for further 10 min and heated at 85 °C for overnight. The reaction mass was concentrated and the reside diluted with water and extracted with ethyl acetate . The combined organic extracts were washed with brine solution and dried over anhydrous sodium sulphate. The organic layer was evaporated under reduced pressure to obtain the crude product which was purified by 60-120 mesh silica gel column chromatography using 25% Ethyl acetate ; hexanes mixture to obtain 3-(4-(tert- butoxycarbonyl)piperazin-1-yl)-5-fluorobenzoic acid (1.500 g, 71.8 %) an oil. m/z (ES-), M- = 323

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-d16088bf6acb4600ad776547cf486a02
Quellennotiz750 AstraZeneca ELN dataset