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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705984Generated: October 31, 2026

Trifluoroacetic acid → 2-[3-Bromo-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl]-ethylamine

https://huagongshe.com/reaction/705984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant{2-[3-Bromo-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67776337—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-[3-Bromo-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl]-ethylamineHCID 6777612899.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

{2-[3-bromo-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl]-ethyl}-carbamic acid tert-butyl ester (1.3 g, 2.818 mmol) was dissolved in dichloromethane (10 ml) and stirred at 0° C. for 5 min. TFA (1.08 ml, 14.091 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-[3-bromo-(5-trifluoromethyl-pyridin-2-yloxy)-phenyl]-ethylamine (1.01 g, 2.796 mmol, yield=99%, purity=100%). [M+H]+=361.17

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-fb4880f7c75d4542ad1ede73e31ddd63
Source noteuspto-grants-2015_11