HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 4-(2-Fluoro-2-(4-tert-butylphenyl)ethoxy)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 4-(2-p-Toluenesulfonyloxy-2-(4-tert-butylphenyl)ethoxy) quinazoline | HCID 59678612 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Fluoro-2-(4-tert-butylphenyl)ethoxy)quinazoline | HCID 59678689 | — |
Reaction Steps
A 15 ml round bottom flask is charged with 4-(2-p-toluenesulfonyloxy-2-(4-tert-butylphenyl)ethoxy)quinazoline (0.3 g, 0.84 mmol). Tetrabutylammonium fluoride solution (1M in THF, 4.2 ml, 4.2 mmol) is then added to it and the solution is heated at reflux for 60 minutes. The mixture is then cooled and water is added to it. It is then extracted with dichloromethane, washed with water and dried. The crude obtained after concentration is purified by silica gel flash chromatography (ethyl acetate/hexanes) to obtain the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09161997B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-d2e842c6575b43f79b2490543774e898 |
| Source note | uspto-grants-2015_10 |