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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650337Generated: October 30, 2026

Acetonitrile → HCID 14418677, compound

https://huagongshe.com/reaction/1650337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
Reactant2-ChloroacrylonitrileHCID 70198—
ReactantHCID 86743902HCID 86743902—
ProductHCID 14418677HCID 1441867768.5%

Reaction Steps

83.8 g (0.6 mole) of 1-dimethylamino-1-aza-3-isopropyl-1,3-butadiene and 121.4 g (1.2 moles) of triethylamine are dissolved in 325 ml of acetonitrile. To this solution are added 52.5 g (0.6 mole) of α-chloroacrylonitrile. This solution is heated for 4 hours to 70° C., cooled, filtered, and concentrated by evaporation. The oily residue is dissolved in dioxane and gaseous HCl is introduced into the solution with ice cooling until the pH is 1. After 30 minutes, the batch is concentrated by evaporation and the residue is partitioned between chloroform and 1N NaHCO3. The organic phase is dried and concentrated by evaporation. The residual oil is distilled under a high vacuum at 81°-84° C. The distillate solidifies, affording 60.1 g (68.5%) of the title compound with a melting point of 47°-49° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923993
Source datasetuspto-grants-1990_05
ORD IDord-69823c8bf6fa41b6971f6b7d8349a8bc
Source noteuspto-grants-1990_05