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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084292Generated: October 26, 2026

Acrylonitrile → 3-(n-Decylthio)propionitrile

https://huagongshe.com/reaction/1084292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
Reactant1-DecanethiolHCID 8917—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product3-(n-Decylthio)propionitrileHCID 15709042—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a 250 mL round-bottomed flask fitted with an overhead mechanical stirrer, a thermometer and an addition funnel were charged 87 g of 1-decanethiol and 20 drops of a 21% by weight solution of sodium ethoxide in ethanol. The mixture was cooled to 10° C. using an ice bath. Then the dropwise addition of 53 g of acrylonitrile was started. After addition of a portion of the acrylonitrile, 10 drops of 21% by weight solution of sodium ethoxide in ethanol were added. The temperature of the reaction mixture during the addition of the remaining acrylonitrile ranged between 30° C. and 35° C. The reaction mixture was then kept at room temperature overnight (~19 hours). The unreacted acrylonitrile was then removed by distillation at atmospheric pressure. The remaining material was then distilled at ~1 mm pressure. A first fraction was collected from 150° C. to 160° C. Fraction one had a strong odor of thiol. A second and final fraction was collected at 160° C. The second fraction had a faint odor of thiol. An NMR spectrum indicated the second fraction to be the desired product 83.5% of theoretical (94.9 g) based upon the weight of 1-decanethiol employed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004558
Source datasetuspto-grants-1991_04
ORD IDord-94864048d2574671bf6b2fdae4cd2713
Source noteuspto-grants-1991_04