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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696283Generated: October 26, 2026

Iodine → Ethyl 5-benzylnicotinate

https://huagongshe.com/reaction/1696283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBenzyl BromideHCID 7498—
ReactantEthyl 5-bromopyridine-3-carboxylateHCID 140785—
ReactantSodium BicarbonateHCID 516892—
CatalystZincHCID 23994—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductEthyl 5-benzylnicotinateHCID 66610002—

Reaction Conditions

Temperature80 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163766B2
Source datasetuspto-grants-2012_04
ORD IDord-ddf95e2923374593852dbd9c901bf83b
Source noteuspto-grants-2012_04