HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Tert-butyl 4-(3-(4-amino-3-(trifluoromethyl)phenoxy) propyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Tert-butyl 4-(3-(4-nitro-3-(trifluoromethyl)phenoxy)propyl)piperazine-1-carboxylate | HCID 59349553 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl 4-(3-(4-amino-3-(trifluoromethyl)phenoxy) propyl)piperazine-1-carboxylate | HCID 59349411 | — |
Reaction Steps
A flask was charged with tert-butyl 4-(3-(4-nitro-3-(trifluoromethyl)phenoxy)propyl)piperazine-1-carboxylate (0.78 g, 1.8 mmol), ammonium formate (0.45 g, 7.2 mmol), and iron powder (0.40 g, 7.2 mmol). Toluene (15 mL) and water (15 mL) were added to the flask and the mixture was heated to reflux for 2 hours, after which time, the hot mixture was filtered through a plug of Celite. The solvent was removed on a rotary evaporator under reduced pressure to yield tert-butyl 4-(3-(4-amino-3-(trifluoromethyl)phenoxy) propyl)piperazine-1-carboxylate. The material was used without further purification. MS (EI): 404 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088767B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-23d8633550924736af59b4ac62b46501 |
| Source note | uspto-grants-2012_01 |