Réaction #2271
ord-351246f0dd44448ebbd806606156bbea
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températureheated to 70°-80° C. during 5.5 hours, during which time the mixture
- 2TempératureThe reaction mixture was cooled
- 3workup.ADDITIONpoured slowly
- 4workup.ADDITIONIce was added intermittently during this addition
- 5Températureto maintain the temperature below 15° C
- 6Températurethe resulting mixture heated at 100° C. for one hour
- 7TempératureThe mixture was cooled
- 8AutreThe two resulting layers were separated
- 9Extractionthe aqueous layer extracted with toluene (2×100 ml)
- 10LavageThe combined organic layers were washed with water (5×200 ml)
- 11Séchagedried over anhydrous sodium sulfate
- 12AutreThe solvent was evaporated in vacuo
- 13Autrethe resulting yellow solid was triturated with hexane
Mode opératoire
Phosphorus oxychloride (92 g) was added dropwise to stirred DMF (78 ml) between 10°-15° C. To the resulting slurry was added 4-chlorophenylacetic acid (34.12 g). The resulting mixture was stirred at room temperature for one half hour and then heated to 70°-80° C. during 5.5 hours, during which time the mixture became effervescent. The reaction mixture was cooled and poured slowly onto cracked ice. The resulting suspension was brought to pH 10 with solid potassium carbonate. Ice was added intermittently during this addition to maintain the temperature below 15° C. Toluene (150 ml) was added and the resulting mixture heated at 100° C. for one hour. The mixture was cooled and allowed to stand overnight. The two resulting layers were separated and the aqueous layer extracted with toluene (2×100 ml). The combined organic layers were washed with water (5×200 ml) and dried over anhydrous sodium sulfate. The solvent was evaporated in vacuo and the resulting yellow solid was triturated with hexane to yield 26 g of 2-(4-chlorophenyl)-3-dimethylaminopropenal as a tan solid mp. 120°-125° C.