HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → N-(3-ethoxycarbonylpropyl)-N-(2-bromoethyl)-N-[2-(chroman-3-yl)ethyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine | HCID 14838465 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-ethoxycarbonylpropyl)-N-(2-bromoethyl)-N-[2-(chroman-3-yl)ethyl]amine | HCID 14838456 | — |
Reaction Steps
29.1 g (0.1 mol) of N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine are dissolved in 200 ml of methanol, and then 10.5 g (0.1 mol) of triethylamine and 18.8 g (0.1 mol) of 1,2-dibromoethane are added to the solution. The reaction mixture is stirred for 16 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-(3-ethoxycarbonylpropyl)-N-(2-bromoethyl)-N-[2-(chroman-3-yl)ethyl]amine is thus obtained in the form of an oil which can be used further in the crude state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04957928 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-1ee38fbd93924f0995ef47649dda00ab |
| Source note | uspto-grants-1990_09 |