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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantIsopropylamineHCID 6363—
ReactantHCID 21196139HCID 21196139—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-isopropyl-4-(2-fluoro-5-bromobenzyloxy)butylamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-d75da251196b47598d465cad33e98cc8
Source noteuspto-grants-2001_06