Réaction #7239
ord-b0ed2b81d0864736adc41f19e2b2dd94
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températurethe solution was heated at 70° C. overnight
- 2Températureto cool to room temperature
- 3Concentrationconcentrated under reduced pressure
- 4workup.DISSOLUTIONThe residue was dissolved in CHCl3 (100 mL)
- 5workup.ADDITIONtreated with solid Na2CO3 (14.12 g)
- 6workup.WAITAfter 1 hour
- 7Autrethe supernatant was decanted
- 8Lavagethe residue was washed with warm CHCl3 (3×50 mL)
- 9FiltrationThe combined supernatants were filtered
- 10Concentrationconcentrated
- 11Autreto provide 4.6951 g as a yellow solid
- 12Températureheated at 90° C. overnight
- 13TempératureThe mixture was cooled to room temperature
- 14Concentrationconcentrated
- 15Filtrationthe crude product was filtered through a silica plug (33 g silica, ethyl acetate)
Mode opératoire
To a stirred solution of 2,3-lutidine (4.8363 g, 45.13 mmol) in glacial acetic acid (30 mL) at room temperature was added 30% H2O2 (4.6 mL) and the resultant solution was heated to 70° C. After 6 hours, the reaction mixture was cooled to room temperature, additional H2O2 (4.6 mL) was added, and the solution was heated at 70° C. overnight. The reaction mixture was allowed to cool to room temperature and then concentrated under reduced pressure. The residue was dissolved in CHCl3 (100 mL) and treated with solid Na2CO3 (14.12 g). After 1 hour, the supernatant was decanted and the residue was washed with warm CHCl3 (3×50 mL). The combined supernatants were filtered and concentrated to provide 4.6951 g as a yellow solid. The solid was dissolved in acetic anhydride (38 mL) and heated at 90° C. overnight. The mixture was cooled to room temperature and concentrated and the crude product was filtered through a silica plug (33 g silica, ethyl acetate) to give 6.13 g of 2-acetoxymethyl-3-methyl-pyridine as an orange oil.