HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 4-(2-Chloro-1,1-difluoroethoxy)benzeneamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Dichloro-1,1-difluoroethane | HCID 15442 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Chloro-1,1-difluoroethoxy)benzeneamine | HCID 19792700 | — |
Reaction Steps
2.5 g (22.9 mmol) of p-aminophenol, 3.09 g (22.9 mmol) of 1,2-dichloro-1,1-difluoroethane, 5.48 g (39.6 mmol) of K2CO3 and 40 ml of dry acetonitrile were stirred together at room temperature for 5 days. The mixture was poured into water and extracted two times into ether. The combined ether extracts were washed with water, dried over MgSO4 and filtered: HCl gas was bubbled into the ether solution causing the above-named aniline to precipitate as the hydrochloride salt, which was collected by filtration and recrystallized twice from CH3CN to give 0.9 g (16 percent of theoretical d 245°-250° C.) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250690 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-c511a8c8feb8478d9e51ff3b4f62f5c5 |
| Source note | uspto-grants-1993_10 |