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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406469Generated: October 29, 2026

Toluene → 2-Amino-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanone

https://huagongshe.com/reaction/406469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrifluoroacetic acidHCID 6422—
Reactant{2-Oxo-2-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethyl}-carbamic acid tert-butyl esterHCID 59764640—
SolventDichloromethaneHCID 6344—
Product2-Amino-1-[3-(4-phenylpiperidin-1-yl)pyrrolidin-1-yl]ethanoneHCID 5976469597%

Reaction Steps

To a solution of {2-oxo-2-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethyl}-carbamic acid tert-butyl ester (preparation #10) (3.25 g, 8.39 mmol) in DCM (200 mL) was added TFA (15 mL). The reaction mixture was stirred at ambient temperature for about 5 h. Toluene (100 mL) was added and the solvents were removed in vacuo. The residue was dissolved in DCM (400 mL) and the organic was washed with saturated NaHCO3, 1.0N NaOH, brine, dried over MgSO4, filtered and concentrated in vacuo to give 2-amino-1-[3-(4-phenyl-piperidin-1-yl)-pyrrolidin-1-yl]-ethanone (2.34 g, 97%) as a light tan solid; RP-HPLC (Table 1, Method a) Rt 1.09 min; m/z: (M+H)+ 288.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754107B2
Source datasetuspto-grants-2014_06
ORD IDord-d722e188075147e18a2098c6de752165
Source noteuspto-grants-2014_06