Réaction #1519074
ord-6e4271858e7d42cfa2f6e9b2657c0378
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1workup.ADDITIONDuring the addition the reaction
- 2workup.ADDITIONafter addition
- 3workup.ADDITIONwas added
- 4Autrethe temperature below −50° C
- 5TempératureThe reaction was warmed to room temperature
- 6workup.WAITwas continued for 2 hours
- 7AutreThe phases were separated
- 8Concentrationthe organic phase concentrated
- 9LavageThe solution was washed twice with 500 mL of aqueous 10% HCl
- 10SéchageThe organic phase was dried over MgSO4
- 11Filtrationfiltered
- 12Concentrationconcentrated to 372 g of a light gold oil (93% pure by GC)
- 13workup.DISTILLATIONThis oil was distilled bulb to bulb
Mode opératoire
To a solution of 2-chloro-6-fluoroanisole (321.2 g) in 2 L of dry tetrahydrofuran (THF), cooled to −70° C., was added 890 mL of 2.5 M n-BuLi in hexane over 30 min with good mechanical stirring. During the addition the reaction warmed to −48 to −50° C. and was held there for 15 min after addition was complete. The solution was cooled to −75° C. before a solution of 177 g of dimethylformamide (DMF) in 100 mL of THF was added keeping the temperature below −50° C. The reaction was warmed to room temperature and 260 g of 37% aqueous HCl was slowly added and stirring was continued for 2 hours. The phases were separated and the organic phase concentrated and taken into 2 L of ether. The solution was washed twice with 500 mL of aqueous 10% HCl. The organic phase was dried over MgSO4, filtered and concentrated to 372 g of a light gold oil (93% pure by GC). This oil was distilled bulb to bulb to give 282 g (75% yield) of a light gold oil that solidified upon standing. A small sample was crystallized from pentane to give fine white needles; MP 44-45° C.; 1H NMR (CDCl3, 300 MHz) δ 10.3 (s, 1H); 7.5 (dd, 1H, J=6.6, 8.5 Hz); 7.3 (m, 1H); 4.0 (s, 3H).