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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843900Generated: November 2, 2026

Potassium Iodide → 7-Iodo-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/1843900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl AcetateHCID 8857—
Reactant7-Amino-1,2,3,4-tetrahydroisoquinolin-1-oneHCID 13152844—
ReactantSodium NitriteHCID 23668193—
CatalystCopper iodideHCID 83717—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product7-Iodo-3,4-dihydroisoquinolin-1(2H)-oneHCID 1054016147.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaNO2 (340 mg, 4.9382 mmol) was added to a solution of 7-amino-3,4-dihydro-2H-isoquinolin-1-one (I-32a: 800 mg, 4.9382 mmol) in concentrated HCl (2 mL) and water (2 mL) at 0° C. The reaction mixture was stirred at 0° C. for 15 minutes. The resulting diazonium salt solution was added portion wise to a vigorously stirred biphasic mixture of DCM (25 mL), potassium iodide (4.9 g, 29.6242 mmol), copper iodide (47 mg, 0.25 mmol) and water (8 mL). The resulting mixture was stirred at room temperature overnight. The reaction was monitored by TLC (80% ethylacetate in hexane). The reaction mixture was diluted with DCM. The organic layer was washed with 10% Na2S2SO3 solution, dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (50% ethylacetate in hexane) afforded 640 mg of the product (44.50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946260B2
Source datasetuspto-grants-2015_02
ORD IDord-f9979c4512e048348d5cd4f06df08328
Source noteuspto-grants-2015_02