Réaction #417931
ord-4e6c8315e1c24b419d87d559db6b4539
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températurethe mixture was heated
- 2TempératureHeating
- 3Autrewas removed
- 4workup.ADDITIONtoluene was added (30 ml)
- 5workup.STIRRINGStirring
- 6workup.WAITwas continued for 15 min
- 7Autreto obtain a brown solution, which
- 8Températurewas cooled with an ice bath
- 9workup.STIRRINGThe resulting biphasic mixture was further stirred until it
- 10Autrereached room temperature
- 11LavageThe organic layer was washed 3 times with water
- 12Lavageby washing three times with half saturated aq. NaCl
- 13Séchagedried over MgSO4
- 14Concentrationconcentrated in a rotary evaporator
- 15Autreto obtain 9.44 g (73%) of crude brown oil, which
- 16workup.DISTILLATIONwas short-path distilled at 129° C./0.05 mbar
Mode opératoire
p-Tolyl 3-phenylpropanoate (13.0 g, 54.1 mmol) was added to aluminium chloride (9.38 g, 70.3 mmol) and the mixture was heated under stirring to 178° C. for 2 h. Heating was removed and toluene was added (30 ml). Stirring was continued for 15 min to obtain a brown solution, which was cooled with an ice bath prior to the careful, dropwise addition of water (30 ml). The resulting biphasic mixture was further stirred until it reached room temperature, then diluted with toluene. The organic layer was washed 3 times with water, then twice with 1N aq. NaOH solution (50 ml). The organic layer was then neutralized by washing three times with half saturated aq. NaCl, then dried over MgSO4 and concentrated in a rotary evaporator to obtain 9.44 g (73%) of crude brown oil, which was short-path distilled at 129° C./0.05 mbar to obtain 1-(2-hydroxy-5-methylphenyl)-3-phenylpropan-1-one (4.39 g, 34%). The product was further purified by column flash chromatography on silica to obtain 3.68 g (28%) of product, which was finally recrystallized from hexane to yield 2.93 g (25%) of product as white crystals, melting point 40.3° C.