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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474737Generated: October 25, 2026

Trifluoroacetic acid → 2-[4-(3-Chloro-4-trifluoromethyl-phenoxy)-phenyl]-ethylamine

https://huagongshe.com/reaction/474737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant{2-[4-(3-Chloro-4-trifluoromethyl-phenoxy)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67774227—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-[4-(3-Chloro-4-trifluoromethyl-phenoxy)-phenyl]-ethylamineHCID 6777546272%

Reaction Conditions

Temperature0 °C

Reaction Steps

Entire reaction was performed under argon atmosphere using syringe septa technique. {2-[4-(3-chloro-4-trifluoromethyl-phenoxy)-phenyl]-ethyl}-carbamic acid tert-butyl ester (3.703 mmol, 1 eq) was dissolved in dichloromethane (20 ml) and stirred at 0° C. for 5 min. TFA (18.517 mmol, 5 eq) was added and stirring was continued overnight. Reaction mixture was diluted with 10 ml NaHCO3 (sat.) and extraction with DCM (3×20 ml) followed. Organic layers were combined and evaporated in vacuo to give 2-[4-(3-chloro-4-trifluoromethyl-phenoxy)-phenyl]-ethylamine (2.661 mmol, yield=72%, purity=99%). [M+H]+=316.21 1H NMR (300 MHz, CDCl3) δ/ppm 2.68-2.82 (m, 2H), 2.91-3.05 (m, 2H), 6.81-6.91 (m, 1H), 6.93-7.07 (m, 4H), 7.16-7.23 (m, 1H), 7.52-7.63 (m, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-96557fd836fc4e15be1c2e79ff491a77
Source noteuspto-grants-2014_01