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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717514Generated: October 25, 2026

Sodium → (5-Fluoro-2-phenoxy-phenyl)-{5-methoxy-2-[2-(mesyloxy-)-ethoxy]-benzyl}-amine

https://huagongshe.com/reaction/1717514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
Reactant5-Fluoro-2-phenoxyanilineHCID 19627132—
Reactant5-Methoxy-2-(2-mesyloxyethoxy)-benzaldehydeHCID 59765855—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
Product(5-Fluoro-2-phenoxy-phenyl)-{5-methoxy-2-[2-(mesyloxy-)-ethoxy]-benzyl}-amineHCID 8662178762%

Reaction Steps

To stirred solution of 9.1 g (45 mmol) 1b, 12.3 g (45 mmol) 4a and one drop of glacial acid in 60 ml dichloroethane (pH=5) were added 14.8 g (70 mmol) sodium tris-acetoxy hydro borane. The reaction mixture was stirred over night and diluted with 5 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 4b was obtained in 62% yield (12.9 g, 27.9 mmol) as yellow oil. The crude product 4b was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803960B2
Source datasetuspto-grants-2010_09
ORD IDord-787d6f34270a46d5a6eeb4857bbad118
Source noteuspto-grants-2010_09