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1-Pyrrolidineethanol,hydrochloride (1:1) synthesis

2synthesis methods
2713-34-0 Synthesis
3,5-Difluorophenol

2713-34-0
392 suppliers
$5.00/1g

1-Pyrrolidineethanol,hydrochloride (1:1)

30727-31-2
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Pyrrolidine, 1-[2-(3,5-difluorophenoxy)ethyl]-

660432-42-8
1 suppliers
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Yield:660432-42-8 50%

Reaction Conditions:

with caesium carbonate;sodium iodide in DMF (N,N-dimethyl-formamide) at 20;

Steps:

91.A Preparation 91; 2, [6-DIFLUORO-4- (PYRROLIDIN-1-YL-ETHOXY)-BENZALDEHYDE]; A. [1-(35-DIFLUORO-PHENOXAMETHYL)-PYRROLIDINE]

Add [PYRROLIDIN-1-YL-ETHANOL] hydrochloride (1.5 g) to a mixture of 3,5- difluorophenol (1.0 g), cesium carbonate (8. [78] g), sodium iodide (1.15 g) in dry dimethylformamide (20 mL). Stir at room temperature overnight. Concentrate under reduced pressure and the residue is purified by chromatography eluting with ethyl acetate: hexane (1: 1) to provide (0.8 g, 50%) of an oil.

References:

WO2004/14900,2004,A1 Location in patent:Page 50-51