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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 7-Amino-1,2,3,4-tetrahydroisoquinolin-1-one | HCID 13152844 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 7-Iodo-3,4-dihydroisoquinolin-1(2H)-one | HCID 10540161 | 47.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946260B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f9979c4512e048348d5cd4f06df08328 |
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| Source note | uspto-grants-2015_02 |
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