Reaktion #156306

Reaktionsgleichung

hydrochloric acid

di-tert-butyl azodicarboxylate

triphenylphosphine

(3R)-1-methylpyrrolidin-3-ol

→

(3S)-3-hydrazino-1-methylpyrrolidine dihydrochloride

Lösungsmittel

tetrahydrofuran

tetrahydrofuran

water

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturunder ice-cooling
2. 2
   workup.STIRRINGfurther stirring at room temperature for 1 hour
3. 3
   workup.STIRRINGby stirring at room temperature overnight
4. 4
   Sonstigewas evaporated under reduced pressure
5. 5
   workup.ADDITION20 mL of dichloromethane was added
6. 6
   Sonstigethe organic layer was separated
7. 7
   WaschenThe obtained aqueous layer was washed with 20 mL of dichloromethane twice
8. 8
   Sonstigethe aqueous layer was evaporated under reduced pressure
9. 9
   SonstigeAfter forming a precipitate
10. 10
    Filtrationthe obtained solid was collected by filtration
11. 11
    Sonstigedried under reduced pressure

Vorschrift

To a mixture of (3R)-1-methylpyrrolidin-3-ol and 35 mL of tetrahydrofuran was added 18.2 g of triphenylphosphine, and a solution of 13.2 g of di-tert-butyl azodicarboxylate in 10 mL of a tetrahydrofuran was added dropwise thereto under ice-cooling, followed by stirring for 1 hour, and further stirring at room temperature for 1 hour. To the reaction mixture was added 40 mL of a 6 M hydrochloric acid, followed by stirring at room temperature overnight. To the reaction mixture was added 40 mL of water, tetrahydrofuran was evaporated under reduced pressure, and then 20 mL of dichloromethane was added thereto and the organic layer was separated. The obtained aqueous layer was washed with 20 mL of dichloromethane twice, and the aqueous layer was evaporated under reduced pressure, and then coevaporated with isopropanol. After forming a precipitate, the obtained solid was collected by filtration and dried under reduced pressure to obtain 7.92 g of (3S)-3-hydrazino-1-methylpyrrolidine dihydrochloride.

Quelle