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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066831Generated: November 1, 2026

Sodium Iodide → N-ethyl-4-(2-fluoro-5-bromobenzyloxy)butylamine

https://huagongshe.com/reaction/1066831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantEthylamineHCID 6341—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 21196139HCID 21196139—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductN-ethyl-4-(2-fluoro-5-bromobenzyloxy)butylamineHCID 21196011—

Reaction Steps

A solution of 4-(2-fluoro-5-bromobenzyloxy)butyl bromide (500 mg, 1.47 mmol) in acetone (7.3 ml) was treated with sodium iodide (242 mg, 1.6 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 ethylamine (11 ml, 22.0 mmol). The resulting mixture was stirred for about 17 hours at ambient temperature. The progress of the reaction was monitored by thin layer chromatography. 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 radial chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-06af627d24274b8e9f33a461fd1da708
Source noteuspto-grants-2001_06