Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 849261Erstellt: 24. Oktober 2026

proline dl-form → HCID 54445738, Verbindung

https://huagongshe.com/de/reaction/849261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktproline dl-formHCID 614—
EduktTriethylamineHCID 8471—
EduktPotassium CarbonateHCID 11430—
EduktTriethylamine hydrobromideHCID 12493—
Edukt1,4-Dibromo-2-fluorobenzeneHCID 137004—
EduktHCID 86755020HCID 86755020—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelN,N-Dimethylformamide--water (1/1)HCID 21962138—
ProduktHCID 54445738HCID 54445738—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a solution of DL-proline (576 mg, 5 mmol) in 10/1 DMF-H2O (7.5 ml) at RT were added CuI (48 mg, 0.25 mmol), Pd(PPh3)4 (290 mg, 0.25 mmol), K2CO3 (690 mg, 5 mmol), NEt3 (1.4 ml, 10 mmol), triethylammonium bromide (158 mg, 0.75 mmol), and 1,4-dibromo-2-fluorobenzene. The resulting mixture was stirred in a sealed tube at 120° C. for 48 hours. The reaction mixture was cooled to room temperature and poured onto saturated K2CO3 /Et2O. The aqueous layer was extracted 3× with Et2O. The pH of the aqueous layer was adjusted to 4 and extracted 3× with EtOAc. The combined organics were washed with brine, dried over MgSO4, and concentrated in vacuo to produce title compound which was used without further purification: LCMS (M+1)=287. ##STR393##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06011059
Quelldatensatzuspto-grants-2000_01
ORD IDord-8ddff6181fa046e180dda31bb25f3ba9
Quellennotizuspto-grants-2000_01