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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429365Generated: October 31, 2026

Trifluoroacetic acid → 1((2-(Bromomethyl)benzyl)oxy)-3-(4-bromophenyl)propan-2-amine trifluoroacetic acid salt

https://huagongshe.com/reaction/1429365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl(1-((2-(bromomethyl)benzyl)oxy)-3-(4-bromophenyl)propan-2-yl)carbamateHCID 123844053—
SolventDichloromethaneHCID 6344—
Product1((2-(Bromomethyl)benzyl)oxy)-3-(4-bromophenyl)propan-2-amine trifluoroacetic acid saltHCID 6738225295%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of compound 3i (2.2 g, 4.3 mmol) in DCM (20 mL) was added slowly TFA (2 mL) at 0° C. The mixture was stirred at 0° C. for 2 hr. LCMS analysis indicated the total consumption of compound 3i. The solvent was removed in vacuum to give 3k as a white solid (1.68 g, 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940722B2
Source datasetuspto-grants-2015_01
ORD IDord-2acb14afbf5a4ad8995a72ace2448417
Source noteuspto-grants-2015_01