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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196036Generated: October 26, 2026

Acrylonitrile → N-[2-(chroman-3-yl)ethyl]-N-(2-cyanoethyl)-N-(2-methoxycarbonylethyl)amine

https://huagongshe.com/reaction/1196036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantTriethylamineHCID 8471—
ReactantN-[2-(chroman-3-yl)ethyl]-N-(2-methoxycarbonylethyl)-amine hydrochlorideHCID 14838449—
SolventMethanolHCID 887—
ProductN-[2-(chroman-3-yl)ethyl]-N-(2-cyanoethyl)-N-(2-methoxycarbonylethyl)amineHCID 14838450—

Reaction Steps

30 g (0.1 mol) of N-[2-(chroman-3-yl)ethyl]-N-(2-methoxycarbonylethyl)-amine hydrochloride are dissolved in 100 ml of methanol, and then 10.5 g (0.1 mol) of triethylamine and 5.84 g (0.11 mol) of acrylonitrile are added to the solution and the whole is stirred for 15 hours at room temperature. The reaction mixture is then concentrated under a water-jet vacuum, the residue is taken up in diethyl ether and the ethereal solution is washed neutral with ice-water. The ethereal phase is dried over potassium carbonate and concentrated by evaporation. N-[2-(chroman-3-yl)ethyl]-N-(2-cyanoethyl)-N-(2-methoxycarbonylethyl)-amine is thus obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112855
Source datasetuspto-grants-1992_05
ORD IDord-3808efa6fb6b4c60a92bdbca41bc7118
Source noteuspto-grants-1992_05