HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207188Generated: November 2, 2026
Sodium Iodide → (2E)-2-[(3-iodo-4-pyridyl)methylene]-6-methoxy-tetralin-1-one
https://huagongshe.com/reaction/2207188
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1-N,2-N-dimethylcyclohexane-1,2-diamine | HCID 551074 | — |
| Reactant | (2E)-2-[(3-bromo-4-pyridyl)-methylene]-6-methoxy-tetralin-1-one | HCID 118557971 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2E)-2-[(3-iodo-4-pyridyl)methylene]-6-methoxy-tetralin-1-one | HCID 118557939 | 90% |
Reaction Steps
In a Schlenk tube, N,N′-dimethyl-1,2-cyclohexanediamine 85% (32 μL, 0.20 mmol) and dioxane (2 mL) were added to a mixture of CuI (19.2 mg, 0.1 mmol), compound 87 (688 mg, 2.0 mmol) and NaI (600 mg, 4.00 mmol). The Schlenk tube was sealed with a Teflon cap and the reaction mixture was stirred at 110° C. for 24 h. After cooling, the resulting suspension was poured into water (20 mL), and extracted with dichloromethane (3×). The combined organic phases were dried over magnesium sulfate and concentrated to dryness. The product was allowed to crystallize at room temperature. The residue was purified by column chromatography on SiO2 (gradient of EtOAc in petroleum ether) to afford the title compound 88 as a yellow solid (Yield 703.8 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376387B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-651f420f366e48b09f50f77e29eba715 |
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| Source note | uspto-grants-2016_06 |
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