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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816279Generated: October 27, 2026

Trifluoroacetic acid → 2-(2-Pyrazinyl)aniline

https://huagongshe.com/reaction/1816279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantTert-butyl 2-(2-pyrazinyl)phenylcarbamateHCID 22493234—
SolventDichloromethaneHCID 6344—
Product2-(2-Pyrazinyl)anilineHCID 22493282104.6%

Reaction Steps

To tert-butyl 2-(2-pyrazinyl)phenylcarbamate (0.62 g, 2.29 mmol), dichloromethane (10 mL), and anisole (1 mL) was added trifluoroacetic acid (10 mL). The reaction mixture was stirred at room temperature under a nitrogen atmosphere for 4 h and allowed to stand at room temperature overnight. The reaction mixture was concentrated in vacuo to give 0.41 g of 2-(2-pyrazinyl)aniline, which was coupled with CMI (0.20 g, 1.3 mmol), under conditions described in the general procedure for CMI couplings, to give 0.022 g of N-(4,5-dihydro-1H-imidazol-2-ylmethyl)-2-(2-pyrazinyl)aniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884801B1
Source datasetuspto-grants-2005_04
ORD IDord-e7ee31c679e040fda62ca9f4dc84f780
Source noteuspto-grants-2005_04