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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066846Generated: November 1, 2026

N,N-dimethyl-4-(2-fluoro-5-bromobenzyloxy)butylamine → N-methyl-4-[2-fluoro-5-bromobenzyloxy]butylamine

https://huagongshe.com/reaction/1066846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-dimethyl-4-(2-fluoro-5-bromobenzyloxy)butylamineHCID 21196124—
Solvent1,1-DichloroethaneHCID 6365—
ProductN-methyl-4-[2-fluoro-5-bromobenzyloxy]butylamineHCID 20662459—

Reaction Steps

In a 10 ml flask, under a nitrogen atmosphere, N,N-dimethyl-4-[2-fluoro-5-bromobenzyloxy]butylamine (215 mg, 0.707 mmol) was dissolved in dichloroethane (2.0 ml). To this solution ACE•Cl (0.305 ml, 2.83 mmol) was added and the resulting mixture was heated to reflux. The reaction mixture was refluxed for four hours. The prgress of the reaciton was monitored by thin layer chromatography. The mixture was refluxed for an additional 16 hours. The solvents were removed in vacuo and the residue was taken up in methanol. The methanol solution was refluxed for 1.5 hours and the solvents were removed by evaporation. The residue 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 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-503bd173f3014c0f95d2b27d3ffb106a
Source noteuspto-grants-2001_06