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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253100Erstellt: 24. Oktober 2026

Iodine → Ethyl 5-benzylnicotinate

https://huagongshe.com/de/reaction/253100

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktBenzyl BromideHCID 7498—
EduktEthyl 5-bromopyridine-3-carboxylateHCID 140785—
EduktSodium BicarbonateHCID 516892—
KatalysatorZincHCID 23994—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
ProduktEthyl 5-benzylnicotinateHCID 66610002—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A suspension of Zn (1.0 g, 15 mmol) and I2 (130 mg, 0.5 mmol) in DMA (15 mL) was stirred vigorously until the red color dissipated (3-5 min). Benzyl bromide (1.7 g, 10 mmol) was introduced and the resulting slurry was heated at 80° C. for 2.5 h at which point Cl2Pd(PPh3)2 (250 mg, 0.35 mmol) and a solution of ethyl-5-bromonicotinate (1.1 g, 5.0 mmol) in benzene (10 mL) were introduced and the reaction was heated at 80° C. for 1 h. The reaction was allowed to cool to room temperature and was diluted with EtOAc (100 mL). The mixture was poured into NaHCO3 (5% aqueous, 100 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic layers were sequentially washed with H2O (3×100 mL) and brine before being dried over Na2SO4. Concentration and purification by silica gel chromatography (hexane→50% EtOAc/hexane) provided the title compound as a brown oil. MS m/z: 242.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872009B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-50cc732d3b0e420b88462e0f014fffc4
Quellennotizuspto-grants-2011_01