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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351470Generated: November 2, 2026

Trifluoroacetic acid → N-(2-phenyl-2-(S)-hydroxyethyl)-4-(2-aminoethyl)aniline trifluoroacetate

https://huagongshe.com/reaction/1351470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-(2-phenyl-2-(S)-hydroxyethyl)-4-(N-Boc-2-aminoethyl)anilineHCID 22986857—
SolventDichloromethaneHCID 6344—
ProductN-(2-phenyl-2-(S)-hydroxyethyl)-4-(2-aminoethyl)aniline trifluoroacetateHCID 22986855—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of N-(2-phenyl-2-(S)-hydroxyethyl)-4-(N-Boc-2-aminoethyl)aniline (2.5 g, 7.0 mmole) in CH2Cl2 (15 mL) was cooled in an ice bath under stream of nitrogen and TFA (15 mL) was slowly added. The reaction mixture was stirred for 2 h at 0° C. and then concentrated in vacuo. The crude product was dissolved in 20% MeCN/H2O and purified by preparative reversed phase HPLC (5 to 2% MeCN/H2O over 50 min; 254 nm; 20 mL/min.), to give N-(2-phenyl-2-(S)-hydroxyethyl)-4-(2-aminoethyl)aniline trifluoroacetate salt 31 as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217738B2
Source datasetuspto-grants-2007_05
ORD IDord-ece4a537a7b74e93906e7009052678b3
Source noteuspto-grants-2007_05