Reaktion #1446545

Reaktionsgleichung

2-benzyl-6-(3-pyrroline-1-yl)pyridine

2-benzyl-6-(pyrrolidine-1-yl)pyridine

N-methylmorpholine-N-oxide

water

sodium thiosulfate

→

target compound

2-Benzyl-6-(cis-3,4-dihydroxypyrrolidine-1-yl)pyridine

Lösungsmittel

2-methyl-2-propanol

acetone

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added dropwise little by
2. 2
   workup.STIRRINGit was further stirred at room temperature overnight
3. 3
   workup.STIRRINGby stirring at room temperature for 30 minutes
4. 4
   ExtraktionThen, the mixture was extracted with ethyl acetate
5. 5
   Waschenthe organic phase was washed with water and brine
6. 6
   Sonstigethe solvent was removed
7. 7
   Wascheneluted with hexane/ethyl acetate (5:1)

Vorschrift

2.3 ml of a 2-methyl-2-propanol solution containing 2.5% osmium tetraoxide was added dropwise little by little into a mixture of 11.8 g of a mixture of 2-benzyl-6-(3-pyrroline-1-yl)pyridine and 2-benzyl-6-(pyrrolidine-1-yl)pyridine, 23.5 g of aqueous 50% N-methylmorpholine-N-oxide solution, 50 ml of acetone and 10 ml of water in an ice bath. After stirring for 2 hours in an ice bath, it was further stirred at room temperature overnight. A aqueous sodium thiosulfate solution was added to the reaction solution, followed by stirring at room temperature for 30 minutes. Then, the mixture was extracted with ethyl acetate, and the organic phase was washed with water and brine, and the solvent was removed. Then, the residue was subjected to silica gel column chromatography and eluted with hexane/ethyl acetate (5:1) and then with ethyl acetate, to give 4.2 g of the target compound.

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