HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643776Generated: October 29, 2026
4-Iodophenol → Methyl 5-[(4-iodophenoxy)methyl]furan-2-carboxylate
https://huagongshe.com/reaction/643776
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Iodophenol | HCID 10894 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 5-(chloromethyl)-2-furoate | HCID 75065 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-[(4-iodophenoxy)methyl]furan-2-carboxylate | HCID 997605 | 28% |
Reaction Steps
A solution of 4-iodophenol (10.08 g, 45.8 mmol) in N,N-dimethylformamide (30 mL) was added to a ice-bath cooled suspension of sodium hydride (60%; 1.65 g, 41.2 mmol) in N,N-dimethylformamide (30 mL). The ice bath was removed and the mixture was stirred for 1 h. The mixture was cooled again to ˜5° C. and a solution of 5-(chloro-methyl)-furan-2-carboxylic acid methyl ester (4.00 g, 22.9 mmol) in N,N-dimethylformamide (60 mL) was added. The reaction mixture was stirred overnight at room temperature, then the solvents were evaporated under reduced pressure and water was added. The mixture was extracted three times with ethyl acetate and the combined organic layers were washed twice with 1 M NaOH, and once each with water and brine. The organic solution was dried (magnesium sulfate) filtered, evaporated, and purified using a Biotage 65 L purification system, eluting with 3% methylene chloride/toluene to give 5-(4-iodo-phenoxymethyl)-furan-2-carboxylic acid methyl ester (2.3 g, 28%) as a white solid, along with some mixed fractions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700632B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-e266bdad59cc47679360c89c19cafd16 |
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| Source note | uspto-grants-2010_04 |
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