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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196041Generated: October 31, 2026

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

https://huagongshe.com/reaction/1196041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantTriethylamineHCID 8471—
Reactant2-(3,4-dihydro-2H-1-benzopyran-3-yl)ethan-1-amineHCID 14838408—
SolventMethanolHCID 887—
ProductN-[2-(chroman-3-yl)ethyl]-N-(2-cyanoethyl)-amineHCID 15027461—

Reaction Steps

17.7 g (0.1 mol) of 3-(2-aminoethyl)chroman 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. The reaction mixture is stirred for 15 hours at room temperature and then concentrated under a water-jet vacuum. The residue is taken up in diethyl ether and 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)-amine is thus obtained in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112855
Source datasetuspto-grants-1992_05
ORD IDord-5c20754dd52d483988551349f5c3804d
Source noteuspto-grants-1992_05