Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097213Generated: October 28, 2026

Ethyl chloroacetate → HCID 59547216, compound

https://huagongshe.com/reaction/1097213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium selenideHCID 73973—
Reactant2-ChloronicotinonitrileHCID 81079—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59547216HCID 5954721677.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a suspension of sodium selenide (0.9 g, 7.2 mmol, prepared from 0.75 g of selenium as described above) in DMF (7 mL) was added a solution of 2-chloropyridine-3-carbonitrile (1 g, 7.2 mmol) in DMF (3 mL) at rt for 5 min and stirred the mixture at 60-70° C. for 2 h. Then ethyl chloroacetate (0.78 mL, 7.22 mmol) was added dropwise to the reaction mixture and again stirred at 60-70° C. for 2 h. Then, a solution of sodium methoxide (0.39 g, 7.2 mmol) in methanol (7 mL) was added dropwise and stirring was continued for 1 h at the same temperature. The mixture was allowed to room temperature (rt) and poured into cold water and stirred for 15 min. The precipitated solid was filtered, washed with water and dried to give the product as a yellow color solid (1.5 g, 77%), mp 194-196° C. 1H NMR (400 MHz, CDCl3): δ 8.65 (1H, dd, J=4.6, 1.4 Hz, H-6), 7.86 (1H, dd, J=8.2, 1.4 Hz, H-4), 7.33 (1H, dd, J=8.2, 4.6 Hz, H-5), 6.04 (2H, br s, —NH2), 4.34 (2H, q, J=7.1 Hz, —COOCH2CH3), 1.38 (3H, t, J=7.1 Hz, —COOCH2CH3); LC-MS (positive ion mode): m/z 269, 271 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143237B2
Source datasetuspto-grants-2012_03
ORD IDord-fa60355edf2645deb10a71f8da756b7e
Source noteuspto-grants-2012_03