HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 2-(3,4-dihydro-2H-1-benzopyran-3-yl)ethan-1-amine | HCID 14838408 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine | HCID 14838465 | — |
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 19.5 g (0.1 mol) of 4-bromobutyric acid ethyl ester are added to the solution. The reaction mixture is stirred for 15 hours at room temperature and is 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. Oily N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine is thus obtained and can be used further in crude form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112855 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-6c382037d0704bc1bbecabd86769aec6 |
| Source note | uspto-grants-1992_05 |