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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878242Generated: November 2, 2026

Trifluoroacetic acid → (2-Chloro-4-iodo-pyridin-3-yl)-methyl-amine

https://huagongshe.com/reaction/878242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(2-Chloro-4-iodo-pyridin-3-yl)-methyl-carbamic acid tert-butyl esterHCID 86670802—
SolventDichloromethaneHCID 6344—
Product(2-Chloro-4-iodo-pyridin-3-yl)-methyl-amineHCID 86670801—

Reaction Steps

To an ice-cold solution of (2-chloro-4-iodo-pyridin-3-yl)-methyl-carbamic acid tert-butyl ester (0.97 g, 2.63 mmol) in CH2Cl2 (5 mL) was added TFA (6.00 g, 4.05 mL, 52.6 mmol) and the solution was stirred at room temperature for 1.5 hours before another TFA (6.00 g, 4.05 mL, 52.6 mmol) was added. After stirring at room temperature for 3 hours the clear solution was evaporated. The residue was taken up in saturated aqueous NaHCO3 solution (50 mL) and CH2Cl2 (30 mL) and the layers were separated. The aqueous layer was extracted twice with CH2Cl2 (30 mL each) and the organic layers were washed with brine, dried over MgSO4, filtered and evaporated. Colorless oil (0.61 g; 86%). MS (ESI): m/z=268.93 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987307B2
Source datasetuspto-grants-2015_03
ORD IDord-bfcd0a3ac72d407d8bf238f0fe4c4df4
Source noteuspto-grants-2015_03