HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066832Generated: October 31, 2026
Sodium Iodide → N-isopropyl-4-(2-fluoro-5-bromobenzyloxy)butylamine
https://huagongshe.com/reaction/1066832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | HCID 21196139 | HCID 21196139 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-isopropyl-4-(2-fluoro-5-bromobenzyloxy)butylamine | HCID 21195982 | — |
Reaction Steps
A solution of 4-(2-fluoro-5-bromobenzyloxy)butyl bromide (1.2 g, 3.53 mmol) in tetrahydrofuran (18 ml) was treated with sodium iodide (484 mg, 3.2 mmol). The resulting mixture was stirred at ambient temperature. After 1.5 hours, the sodium bromide was removed by filtration, and the filtrate concentrated. The residue was treated with a tetrahydrofuran solution of isopropylamine (3.01 ml, 35.3 mmol). The progress of the reaction was monitored by thin layer chromatography. The resulting mixture was stirred for about 18 hours at ambient temperature, after which time an additional 10 equivalents of isopropylamine was added to drive the reaction. The reaction mixture was diluted with methylene chloride, and washed with 25 mM phosphate buffer and brine. The organic fraction was dried over sodium sulfate and the solvents were removed in vacuo. The desired title intermediate 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-d75da251196b47598d465cad33e98cc8 |
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| Source note | uspto-grants-2001_06 |
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