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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878065Generated: October 31, 2026

Phenylacetyl chloride → HCID 67050467, compound

https://huagongshe.com/reaction/1878065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
Reactant5-Aminopyridine-2-carbonitrileHCID 3871395—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 67050467HCID 67050467—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 5-amino-2-cyanopyridine (0.500 g, 4.2 mmol) in dry dichloromethane (20 mL) was added triethylamine (0.637 g, 6.3 mmol) and the mixture was stirred at 0° C. To the reaction mixture phenylacetyl chloride (0.973 g, 6.3 mmol) was added dropwise and stirred at 0° C. for 1 hour and then at room temperature for 24 hours. The reaction mixture was diluted with chloroform (100 mL) and washed with water (150 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated to obtain the crude product, which was purified using column chromatography (silica gel, 20% ethyl acetate in petroleum ether as an eluent) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314103B2
Source datasetuspto-grants-2012_11
ORD IDord-073de9e717b644f197515fc98da01cb0
Source noteuspto-grants-2012_11