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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867550Generated: November 1, 2026

Pyridine → HCID 54554517, compound

https://huagongshe.com/reaction/1867550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
Reactant4-(Hydroxymethyl)benzeneboronic acidHCID 2734706—
ReactantHCID 178418822HCID 178418822—
CatalystCupric acetateHCID 8895—
SolventAmmoniaHCID 222—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 54554517HCID 5455451772.7%

Reaction Steps

3.04 g (20 mmol) of 4-(hydroxymethyl)phenylboronic acid, 1.44 g (10 mmol) of 4-phenylimidazole, 2.8 ml (20 mmol) of triethylamine and 1.64 ml (20 mmol) of pyridine are dissolved in 20 ml of dimethylformamide. 2.72 g (15 mmol) of copper diacetate are added and the mixture is stirred for 24 hours at ambient temperature. It is diluted with 200 ml of dichloromethane and 200 ml of aqueous 28% ammonia solution. After the phases have settled and been separated, the aqueous phase is extracted with 100 ml of dichloromethane. The organic phases are washed with 50 ml of saturated aqueous sodium chloride solution, dried over sodium sulphate and evaporated to dryness. The product is purified by chromatography on silica gel, eluting with a 97/3 then 95/5 mixture of dichloromethane and methanol. The product is recrystallized from a mixture of toluene and diisopropyl ether, to give 1.82 g of product in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632850B2
Source datasetuspto-grants-2009_12
ORD IDord-addbcc95d9ff4249af7edf730275f29c
Source noteuspto-grants-2009_12