HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355377Generated: October 31, 2026
2-Iodophenol → 1-(2-Iodophenoxy)-2-nitrobenzene
https://huagongshe.com/reaction/2355377
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodophenol | HCID 10784 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(2-Iodophenoxy)-2-nitrobenzene | HCID 11279266 | 93.5% |
Reaction Steps
To a solution of 2-iodophenol (11.82 g, 52.7 mmol) and 1-fluoro-2-nitrobenzene (5.0 g, 35.1 mmol) in DMSO (50 mL was added K2CO3 (14.5 g, 105.3 mmol), followed by CsF (8.0 g, 52.7 mmol). The resulting suspension was stirred at 50° C. until no starting material remained (˜5 h), cooled to rt and partitioned between water (50 mL) and CH2Cl2 (50 mL). The water layer was separated and extracted with CH2Cl2 (2×10 mL). The combined organic layers were washed with 1 aq N NaOH (10 mL) and brine, and dried over Na2SO4. Solvent was removed under vacuum to give 1-(2-iodophenoxy)-2-nitrobenzene (11.2 g, 93%) as an oil, which was used for next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754737B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-2e8e1ceb28724a3abf2ada73a0e1e6d2 |
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| Source note | uspto-grants-2010_07 |
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