Reacción #83280
ord-6cc04374b2914c638e36d02d78689a42
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGthe mixture was stirred for 2 hours
- 2workup.ADDITIONwas added
- 3Filtraciónthe mixture was filtered
- 4OtroThe organic layer was separated
- 5Lavadowashed with saturated Na2CO3 (6×)
- 6Extracciónthe basic layer was extracted with CH2Cl2
- 7Extracciónthe CH2Cl2 layer was extracted with 2N NaOH
- 8Extracciónthe mixture was extracted with ether
- 9Concentraciónconcentrated in vacuo
- 10Filtraciónfiltered
- 11Lavadorinsed with hexane
Procedimiento
To a cooled mixture of phthalic anhydride (50 g, 0.34 mol) and aluminum chloride (99 g) in tetrachloroethane (300 mL) was added dropwise 1,3-diethylbenzene (50 g) over 11/4 hours. The mixture was stirred in an ice bath for 30 minutes, additional tetrachloroethane was added, and the mixture was stirred for 2 hours. The reaction mixture was poured into concentrated HCl/ice (1 L), ether (500 mL) was added and the mixture was filtered. The organic layer was separated, washed with saturated Na2CO3 (6×), the basic layer was extracted with CH2Cl2 and the CH2Cl2 layer was extracted with 2N NaOH and the 2N NaOH layer was acidified. The basic layer was acidified with aqueous HCl, this acidic layer was combined with the above acidified 2N NaOH layer and the mixture was extracted with ether. The CH2Cl2 layer and the ether layer were combined and concentrated in vacuo. The residue was slurried with water, filtered and rinsed with hexane to afford 88.8 g (93%) of 2-(2,4-diethylbenzoyl)benzoic acid, m.p. 115°-118° C.