HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707498Generated: October 29, 2026
Sodium Iodide → 4-(Benzyloxy)-2-fluoro-1-iodobenzene
https://huagongshe.com/reaction/707498
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-(Benzyloxy)-1-bromo-2-fluorobenzene | HCID 22273933 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Benzyloxy)-2-fluoro-1-iodobenzene | HCID 118162395 | 89.4% |
Reaction Steps
To a mixed solution of 4-(benzyloxy)-1-bromo-2-fluorobenzene (187 g, 665 mmol) described in Production Example 1-2-4 and 1,4-dioxane (300 mL) were added copper iodide (I) (12.6 g, 66.1 mmol), sodium iodide (200 g, 1.33 mol) and N,N′-dimethylethylenediamine (14.0 mL, 132 mmol) at room temperature, and the resultant mixture was stirred under a nitrogen atmosphere at 110 to 115° C. for 19 hours. The reaction mixture was cooled to room temperature, then water and ethyl acetate were added to the reaction mixture, the resultant mixture was filtrated using Celite, and a filtrate was partitioned between aqueous layer and organic layer. The aqueous layer was extracted with ethyl acetate. The combined organic layers were filtrated using a glass filter having silica gel laid thereon. The silica gel was washed with ethyl acetate, organic layers obtained were combined, and the solvent was evaporated under a reduced pressure. The resultant residue was purified by silica gel column chromatography (heptane:ethyl acetate=7:1 and then 4:1) to give the title compound (195 g, yield: 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174998B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-c93a2aa26c444a06bc299c4ef183aacd |
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| Source note | uspto-grants-2015_11 |
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