Reaction #2213
ord-d54af9d4762649be9b45711704142f42
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1Temperatureheated to 70°-80° C. during 5.5 hours, during which time the mixture
- 2TemperatureThe reaction mixture was cooled
- 3workup.ADDITIONpoured slowly
- 4workup.ADDITIONIce was added intermittently during this addition
- 5Temperatureto maintain the temperature below 15° C
- 6Temperaturethe resulting mixture heated at 100° C. for one hour
- 7TemperatureThe mixture was cooled
- 8OtherThe two resulting layers were separated
- 9Extractionthe aqueous layer extracted with toluene (2×100 ml)
- 10WashThe combined organic layers were washed with water (5×200 ml)
- 11Dryingdried over anhydrous sodium sulfate
- 12OtherThe solvent was evaporated in vacuo
- 13Otherthe resulting yellow solid was triturated with hexane
Procedure
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.