HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209742Generated: October 31, 2026
Sodium Iodide → 4-[5-(4-cyano-3-fluoro-phenoxy)pentyloxy]-N,N-bis(1-methylethyl)benzamide
https://huagongshe.com/reaction/2209742
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-5-chloropentane | HCID 96070 | — |
| Reactant | 2-Fluoro-4-hydroxybenzonitrile | HCID 2734675 | — |
| Reactant | 4-hydroxy-N,N-bis(propan-2-yl)benzamide | HCID 21841472 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[5-(4-cyano-3-fluoro-phenoxy)pentyloxy]-N,N-bis(1-methylethyl)benzamide | HCID 19381499 | — |
Reaction Steps
A stirred solution of 4-hydroxy-N,N-bis(1-methylethyl)benzamide (500 mg, 2.3 mmol) in 5 mL of N,N-dimethylformamide is treated with 1-bromo-5-chloropentane (300 μL, 2.3 mmol) and cesium carbonate (750 mg, 2.3 mmol) and heated for 2 hours. This is treated with a mixture of 2-fluoro-4-hydroxy-benzonitrile, and 60% sodium hydride (92 mg, 2.3 mmol) in 2 mL of N,N-dimethylformaide followed by sodium iodide (1.04 g, 6.9 mmol). The reaction is heated to 70° C. for 6 hours and partitioned between ethyl acetate and water. The organic phase is washed with brine, dried over sodium sulfate, and concentrated in vacuo. The resulting material is purified by chromatography on silica gel (20 g) with 70% ethyl acetate/hexane as the eluent to afford 4-[5-(4-cyano-3-fluoro-phenoxy)pentyloxy]-N,N -bis(1-methylethyl)benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455274 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-8966da142b98419c8f0b4b9ef2ab6e85 |
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| Source note | uspto-grants-1995_10 |
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