HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → N-[2-(chroman-3-yl)ethyl]-N-(2-cyanoethyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(3,4-dihydro-2H-1-benzopyran-3-yl)ethan-1-amine | HCID 14838408 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[2-(chroman-3-yl)ethyl]-N-(2-cyanoethyl)-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112855 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-5c20754dd52d483988551349f5c3804d |
| Source note | uspto-grants-1992_05 |