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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876029Generated: November 2, 2026

Trifluoroacetic acid → 5,6,7,8-Tetrahydroisoquinolin-3-amine

https://huagongshe.com/reaction/1876029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantIsoquinolin-3-AmineHCID 311869—
CatalystAdams' catalystHCID 345198—
Product5,6,7,8-Tetrahydroisoquinolin-3-amineHCID 1330239757%

Reaction Steps

A mixture of isoquinolin-3-amine (239 mg, 1.66 mmol), platinum(IV)oxide (28 mg, 0.123 mmol), and TFA (6 mL) was hydrogenated in the Parr apparatus for 3 hrs. The reaction mixture was filtered with the aid of ethyl acetate. The filtrate was evaporated in vacuo and the residue was partitioned between 10% aqueous sodium carbonate and ethyl acetate. The layers were separated, the aqueous phase was washed again with ethyl acetate, and the combined organic layers were washed with brine and dried over magnesium sulfate. The drying agent was filtered off and the solvent evaporated. The material was purified by column chromatography in ethyl acetate to give 139.8 mg (57%) 5,6,7,8-tetrahydroisoquinolin-3-amine as a yellow-white solid. LCMS RT 0.75 min, MH+=149.1 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.78 (1H, s), 6.26 (1H, s), 4.29 (2H, br. s.), 2.64 (4H, ddd, J=10.6, 5.8, 5.5 Hz), 1.64-1.87 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309577B2
Source datasetuspto-grants-2012_11
ORD IDord-e606d3e13f9749729e1e3385c0bb7781
Source noteuspto-grants-2012_11