Réaction #710500

Équation de réaction

2-chloro-6-(trifluoromethyl)nicotinaldehyde

sodium hydroxide

nitro methane

→

1-[2-chloro-6-(trifluoromethyl)pyridin-3-yl]-2-nitroethanol

Rendement 72.0%

Conditions de réaction

Traitement

1. 1
   AutreThe resulting reaction mixture
2. 2
   AutreAfter completion of reaction
3. 3
   Concentrationthe reaction mixture was concentrated under reduced pressure
4. 4
   Autreto remove nitro methane
5. 5
   Autrequenched with ice water (500 mL)
6. 6
   Extractionextracted with ethyl acetate (2×1.0 L)
7. 7
   LavageThe combined organic layer was washed with water (500 mL), brine (500 mL)
8. 8
   Séchagedried over anhydrous sodium sulfate
9. 9
   Concentrationconcentrated under reduced pressure

Mode opératoire

To a stirred solution of 2-chloro-6-(trifluoromethyl)nicotinaldehyde (Int-17) (70 g, 1.0 eq.) in nitro methane (700 mL) was added sodium hydroxide (6.7 g, 0.5 eq.) at room temperature. The resulting reaction mixture was heated to 100° C. and stirred for 2 h. The progress of the reaction was monitored by TLC. After completion of reaction, the reaction mixture was concentrated under reduced pressure to remove nitro methane quenched with ice water (500 mL) and extracted with ethyl acetate (2×1.0 L). The combined organic layer was washed with water (500 mL), brine (500 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to get pure 1-[2-chloro-6-(trifluoromethyl)pyridin-3-yl]-2-nitroethanol (Int-18) (65.0 g, 72.0%).

Source