Reaktion #313010

Reaktionsgleichung

4-Hydroxy-3-methoxybenzonitrile

triphenylphosphine

tert-butyl (3S)-3-hydroxypyrrolidine-1-carboxylate

diisopropyl azodicarboxylate

→

title compound

Ausbeute 67.0%

3-Methoxy-4-[(3R)-pyrrolidin-3-yloxy]benzonitrile

Ausbeute 67.0%

Lösungsmittel

tetrahydrofuran

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe reaction mixture was then concentrated in vacuo
2. 2
   workup.ADDITIONthe residue was treated with hydrochloric acid (4M in dioxane, 250 mL)
3. 3
   EinengenThe mixture was concentrated in vacuo
4. 4
   Sonstigethe residue was partitioned between ethyl acetate and water
5. 5
   SonstigeThe organic layer was separated
6. 6
   Waschenwashed with water (100 mL)
7. 7
   Waschenthe combined aqueous solution was washed with ethyl acetate (2×150 mL)
8. 8
   Extraktionextracted with ethyl acetate (2×250 mL)
9. 9
   WaschenThe combined organic solution was washed with brine (100 mL)
10. 10
    Trocknendried over magnesium sulfate
11. 11
    Einengenconcentrated in vacuo

Vorschrift

4-Hydroxy-3-methoxybenzonitrile (12 g, 80.2 mmol) and triphenylphosphine (21 g, 80.2 mmol) were added portionwise to an ice-cold solution of tert-butyl (3S)-3-hydroxypyrrolidine-1-carboxylate (15 g, 80.2 mmol) in tetrahydrofuran (225 mL). A solution of diisopropyl azodicarboxylate (16.2 g, 80.2 mmol) in tetrahydrofuran (100 mL) was then added dropwise and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated in vacuo and the residue was treated with hydrochloric acid (4M in dioxane, 250 mL). The mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was separated and washed with water (100 mL), and the combined aqueous solution was washed with ethyl acetate (2×150 mL), basified to pH10 with solid potassium carbonate and extracted with ethyl acetate (2×250 mL). The combined organic solution was washed with brine (100 mL), dried over magnesium sulfate and concentrated in vacuo to afford the title compound as a cream solid in 67% yield, 11.8 g. LRMS ESI m/z 219 [M+H]+

Quelle