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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073917Generated: October 26, 2026

Benzyl Alcohol → Benzyl 2-iodopyridine-5-carboxylate

https://huagongshe.com/reaction/1073917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant6-Iodopyridine-3-carboxylic acidHCID 819062—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-iodopyridine-5-carboxylateHCID 19895696—

Reaction Steps

11 g of 2-iodopyridine-5-carboxylic acid were suspended in 300 ml of dichloromethane and 4 8 g of benzyl alcohol, 10 g of dicyclohexylcarbodiimide and 100 mg of 4-dimethylaminopyridine were added. The mixture was stirred at room temperature and, after 2 hours, filtered. The filtrate was evaporated and the residue was chromatographed on silica gel using firstly ethyl acetate/petroleum ether (1:9) and then ethyl acetate/petroleum ether (1:6) for the elution. There were obtained 12.2 g of benzyl 2-iodopyridine-5-carboxylate which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971982
Source datasetuspto-grants-1990_11
ORD IDord-c47b90a7c8914c9ba406aa6f205d9b5b
Source noteuspto-grants-1990_11