Réaction #2389082

Équation de réaction

ammonium chloride

water

cyclooctanone

Hydroxylamine-O-sulfonic acid

→

2-Azacyclononanone

Rendement 65.0%

Solvants

formic acid

formic acid

Conditions de réaction

Traitement

1. 1
   AutreA 5 L three-neck round bottom flask was fitted with a heating mantle, an overhead mechanical stirrer, an addition funnel
2. 2
   Autreto form a white slurry
3. 3
   workup.ADDITIONAfter the addition
4. 4
   Autrethe addition funnel was replaced by a reflux condenser
5. 5
   Températurethe reaction was heated
6. 6
   Autreto give a brown solution
7. 7
   TempératureAfter the solution was cooled to room temperature
8. 8
   ExtractionThe aqueous mixture was extracted with chloroform (3×1200 mL)
9. 9
   workup.ADDITIONwas added slowly
10. 10
    AutreThe chloroform layer was then separated
11. 11
    Séchagedried over anhydrous sodium sulfate
12. 12
    Autreevaporated under reduced pressure
13. 13
    Autreto afford a
14. 14
    AutreThe oil Was placed in a 5.00 mL round bottom flask with a magnetic stirrer
15. 15
    AutreThe round bottom flask was placed in a silicon oil bath
16. 16
    Autrewas fitted with a short path vacuum distillation head
17. 17
    Autreequipped with a thermometer

Mode opératoire

A 5 L three-neck round bottom flask was fitted with a heating mantle, an overhead mechanical stirrer, an addition funnel, and a thermometer. The reaction was performed under an argon atmosphere. Hydroxylamine-O-sulfonic acid (196.7 g, 1.74 moles, 1.10 equiv.) and formic acid (1 L) were charged into the round bottom flask and stirred to form a white slurry. A solution of cyclooctanone (200.0 g 1.58 moles, 1.0 equiv.) in formic acid (600 mL) was added dropwise to the white slurry via the addition funnel. After the addition, the addition funnel was replaced by a reflux condenser, and the reaction was heated to reflux (internal temperature about 105° C.) for 1 hour to give a brown solution. After the solution was cooled to room temperature, it was poured into a mixture of saturated aqueous ammonium chloride (1.5 L) and water (1.5 L). The aqueous mixture was extracted with chloroform (3×1200 mL). The combined chloroform layers were transferred into a breaker, and saturated sodium bicarbonate (2 L) was added slowly. The chloroform layer was then separated, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to afford a. brown oil. The oil Was placed in a 5.00 mL round bottom flask with a magnetic stirrer. The round bottom flask was placed in a silicon oil bath and was fitted with a short path vacuum distillation head equipped with a thermometer. A Cow-type receiver was connected to three 250 mL flasks. 2-Azacyclononanone (145 g, 65%, mp 64-69° C.) was obtained by vacuum distillation (fraction with head temperature range from 80 to 120° C. at pressures between 3.0 and 3.4 mmHg).

Source