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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415077Generated: October 27, 2026

Toluene → Tert-butyl 4-(3-(4-amino-3-(trifluoromethyl)phenoxy) propyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/415077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAmmonium formateHCID 2723923—
ReactantTert-butyl 4-(3-(4-nitro-3-(trifluoromethyl)phenoxy)propyl)piperazine-1-carboxylateHCID 59349553—
CatalystIronHCID 23925—
SolventWaterHCID 962—
ProductTert-butyl 4-(3-(4-amino-3-(trifluoromethyl)phenoxy) propyl)piperazine-1-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088767B2
Source datasetuspto-grants-2012_01
ORD IDord-23d8633550924736af59b4ac62b46501
Source noteuspto-grants-2012_01