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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717511Generated: October 26, 2026

Sodium → [2-(2-Benzyloxy-ethoxy)-5-methoxy-benzyl]-(5-fluoro-2-phenoxy-phenyl)-amine

https://huagongshe.com/reaction/1717511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
Reactant5-Fluoro-2-phenoxyanilineHCID 19627132—
ReactantHCID 86189517HCID 86189517—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
Product[2-(2-Benzyloxy-ethoxy)-5-methoxy-benzyl]-(5-fluoro-2-phenoxy-phenyl)-amineHCID 6710423378%

Reaction Steps

To stirred solution of 4.6 g (23 mmol) 1b, 6.3 g (23 mmol) 2a and one drop of glacial acid in 35 ml dichloroethane (pH=5) were added 7.4 g (35 mmol) sodium tris-acetoxy hydro borane. The reaction mixture was stirred over night and diluted with 3 ml water. The pH value was adjusted with aqueous sodium hydroxyd solution to pH=8-9. The mixture was extracted three times with dichloromethane. The combined organic phases were washed with water and brine and were dried with magnesium sulfate. The desired crude product 2b was obtained in 78% yield (8.5 g, 17.9 mmol) as yellow oil. The crude product 2b was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803960B2
Source datasetuspto-grants-2010_09
ORD IDord-a33aec81925643d49a17171ce650357a
Source noteuspto-grants-2010_09