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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092170Generated: October 31, 2026

Trifluoroacetic acid → 1-Benzyl-1,2,3,4-tetrahydroquinolin-3-amine

https://huagongshe.com/reaction/2092170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 1-benzyl-1,2,3,4-tetrahydroquinolin-3-ylcarbamateHCID 67236612—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-1,2,3,4-tetrahydroquinolin-3-amineHCID 64031294—

Reaction Steps

Trifluoroacetic acid (3 mL) was added to a solution of (1-benzyl-1,2,3,4-tetrahydroquinolin-3-yl)-carbamic acid tert-butyl ester (481 mg, 1.42 mmol) in dichloromethane (6 mL), stirred for 30 minutes at ambient temperature, and concentrated. A solution of the resulting oil in methanol (10 mL) was treated with potassium carbonate (393 mg, 2.84 mmol), stirred for an hour at room temperature, and concentrated to afford the title compound as yellow residue. MS (DCI/NH3) m/z: 239.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440691B2
Source datasetuspto-grants-2013_05
ORD IDord-b9b4f76b4c9f4a70ab9327bf1337f1c9
Source noteuspto-grants-2013_05