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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878060Generated: November 1, 2026

Chloroacetyl chloride → HCID 67050365, compound

https://huagongshe.com/reaction/1878060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-cyanopyridineHCID 818260—
SolventChloroformHCID 6212—
ProductHCID 67050365HCID 67050365—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2-amino-5-cyanopyridine (2.0 g, 16.8 mmol) in dry chloroform (40 mL) was added triethylamine (2.54 g, 25.21 mmol) with stirring at 0° C. To the reaction mixture chloroacetyl chloride (2.08 g, 18.48 mmol) was added dropwise, and stirred at 0° C. for 1 hour and then at room temperature for 12 hours. The reaction mixture was diluted with chloroform (100 mL) and washed with water (150 mL). The organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The product was recrystallized from chloroform and petroleum ether to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314103B2
Source datasetuspto-grants-2012_11
ORD IDord-906b197ce7f945ba9cda7e9c70151f42
Source noteuspto-grants-2012_11