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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097232Generated: October 29, 2026

Chloroacetonitrile → HCID 59547214, compound

https://huagongshe.com/reaction/1097232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
Reactant2-ChlorobenzonitrileHCID 13391—
ReactantSodium selenideHCID 73973—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59547214HCID 5954721444%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a suspension of sodium selenide (9.14 g, 72.6 mmol, prepared from 5.8 g of selenium as described above) in DMF (72 mL) was added a solution of 2-chlorobenzonitrile (10 g, 72.6 mmol) in DMF (25 mL) at rt for 5 min and stirred the mixture at 100-110° C. for 24 h. Then chloroacetonitrile (5.48 mL, 72.6 mmol) was added dropwise to the reaction mixture and again stirred at 60-70° C. for 2 h. Then, a solution of sodium methoxide (3.9 g, 72.6 mmol) in dry methanol (24 mL) was added dropwise and stirring was continued for 2 h at the same temperature. The mixture was allowed to room temperature (rt) and poured into cold water and stirred for 30 min. The precipitated solid was filtered, washed with water and dried to give the product as an off-white color solid (7 g, 44%), mp 158-160° C. 1H NMR (400 MHz, CDCl3): δ 7.76-7.79 (1H, m, H-7), 7.60-7.63 (1H, m, H-4), 7.41-7.52 (2H, m, H-5,6), 4.90 (2H, br s, —NH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143237B2
Source datasetuspto-grants-2012_03
ORD IDord-4b1804d194cf4748a7121e9900131e9c
Source noteuspto-grants-2012_03