HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49264Generated: October 29, 2026
Sodium hydride → 1-[6-(4-Bromophenoxy)hexyl]-3-(4-fluorophenyl)-2-imidazolidinone
https://huagongshe.com/reaction/49264
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Fluorophenyl)imidazolidin-2-one | HCID 1480785 | — |
| Reactant | HCID 20636597 | HCID 20636597 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[6-(4-Bromophenoxy)hexyl]-3-(4-fluorophenyl)-2-imidazolidinone | HCID 12986487 | — |
Reaction Steps
To a solution of 1-(4-fluorophenyl)-2-imidazolidinone (0.12 g, 0.65 mmol) dissolved in 10 mL dimethylformamide cooled in an ice bath was added NaH (60% dispersion in mineral oil, 39.0 mg, 0.98 mmol). The mixture was stirred at room temperature for 30 minutes and then cooled in ice bath. 1-Bromo-6-(4-bromophenoxy)heptane (0.22 g, 0.65 mmol) was added, and the mixture was stirred at room temperature for additional 4 hours. The reaction was quenched with methanol, and the solvents were removed under reduced pressure. 5 mL of saturated NH4Cl water solution and 10 mL of dichloromethane were added to the residue. The dichloromethane layer was dried over MgSO4, filtered, evaporated, and purified by column chromatography (ethyl acetate:MeOH=10:1) to give the product (i.e., Compound 7) as a white solid (0.14 g, 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706739B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-7070ec48c1e54d5e9696f57c6b0256e5 |
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| Source note | uspto-grants-2004_03 |
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