HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066836Generated: November 1, 2026
Sodium Iodide → 1-[2-Fluoro-5-bromobenzyloxy]-3-[1-(t-butoxycarbonyl)piperidin-3-yl]propane
https://huagongshe.com/reaction/1066836
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (5-Bromo-2-fluorophenyl)methanol | HCID 2773352 | — |
| Reactant | tert-Butyl 3-(3-bromopropyl)piperidine-1-carboxylate | HCID 18515798 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[2-Fluoro-5-bromobenzyloxy]-3-[1-(t-butoxycarbonyl)piperidin-3-yl]propane | HCID 21195954 | — |
Reaction Steps
An amount of 3-[1-(t-butoxycarbonyl)piperidin-3-yl]propyl bromide (180 mg, 0.588 mmol) was dissolved in N,N-dimethylformamide (1.5 ml) in a 10 ml flask under a nitrogen atmosphere. Sodium iodide (176 mg, 1.18 mmol) was added at ambient temperature, and the resulting mixture was stirred for ten minutes. The reaction mixture was treated with 2-fluoro-5-bromobenzyl alcohol (121 mg, 0.588 mmol), delivered as a solution in 0.5 ml of N,N-dimethylformamide. To this mixture was then added sodium hydride (60%, 35 mg, 0.882 mmol) and the resulting mixture was stirred at ambient temperature for three hours. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between 1 M potassium carbonate and methylene chloride. The aqueous fraction was back extracted with methylene chloride. The organic fractions were combined, and dried over sodium sulfate. The solvents were removed in vacuo. The desired title product was further purified by liquid chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245761B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-bccf38b225954f82ae8b946cb5d7aef5 |
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| Source note | uspto-grants-2001_06 |
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