تفاعل #76304
ord-4f64383e7ea34dcaa06e15133f91555f
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةwhile maintaining the pot temperature below 10° C
- 2درجة الحرارةmaintaining the pot temperature below 100° C
- 3درجة الحرارةheated to 40° C
- 4workup.WAITAfter 4 hours
- 5درجة الحرارةthe solution is cooled to room temperature
- 6workup.ADDITIONpoured
- 7أخرىThe organic phase is separated
- 8استخلاصThe aqueous phase is extracted with two 1 L portions of methylene chloride
- 9تجفيفThe combined organics are dried (MgSO4)
- 10تركيزconcentrated
- 11workup.ADDITIONToluene (1 L) is added
- 12تركيزthe solution is concentrated to ca. 500 mL
- 13workup.ADDITIONEthanol (500 mL) is added
- 14درجة الحرارةThe solution is heated to 70° C.
- 15أخرىHCl (g) is bubbled through for 20 minutes
- 16أخرىThe solution is sparged with N2
- 17تركيزconcentrated
- 18أخرىgives
- 19درجة الحرارةis cooled with an ice bath
- 20workup.WAITAfter 1 hour
- 21درجة الحرارةto warm to room temperature
- 22workup.WAITAfter 18 hours
- 23تركيزthe mixture is concentrated
- 24workup.ADDITIONWater (400 mL) and conc. HCl are added (until pH 4)
- 25workup.ADDITIONEthyl acetate (600 mL) is added
- 26أخرىThe organic phase is separated
- 27غسيلwashed with brine
- 28تجفيفdried (MgSO4)
- 29درجة الحرارةThe solution is heated on a steam bath
- 30workup.ADDITIONcharcoal (ca. 3 g) is added
- 31ترشيحThe mixture is filtered through Celite
- 32تركيزconcentrated
- 33workup.DISSOLUTIONThe residue is dissolved in ethyl acetate (300 mL)
- 34درجة الحرارةheptane (600 mL) with heating
- 35workup.ADDITIONSeed crystals are added
- 36درجة الحرارةAfter cooling an organic oil
- 37workup.ADDITIONHeptane (500 mL) is added
- 38درجة الحرارةthe mixture is heated
- 39درجة الحرارةto reflux
- 40workup.ADDITIONtreated with charcoal (ca. 5 g)
- 41ترشيحfiltered
- 42أخرىA solid forms and is collected
- 43workup.ADDITION4:1 mixture of para
- 44أخرىRecrystallization from ethyl acetate/heptane
الإجراء التجريبي
To a slurry of AlCl3 (210 g, 1.6 mol) in methylene chloride (200 mL) cooled in an ice bath is added 4-chlorobutyryl chloride (121 g) dropwise while maintaining the pot temperature below 10° C. After 10 minutes, ethyl benzeneacetic acid (118 g, 0.72 mol) is added dropwise maintaining the pot temperature below 100° C. The mixture is stirred at room temperature for 1 hour, then heated to 40° C. After 4 hours, the solution is cooled to room temperature and poured onto crushed ice (2 L). Methylene chloride (1 L) is added. The organic phase is separated. The aqueous phase is extracted with two 1 L portions of methylene chloride. The combined organics are dried (MgSO4) and concentrated. Toluene (1 L) is added and the solution is concentrated to ca. 500 mL. Ethanol (500 mL) is added. The solution is heated to 70° C. and HCl (g) is bubbled through for 20 minutes. The solution is sparged with N2 and concentrated. Chromatography through silica gel (2.5 L) using an ethyl acetate/heptane gradient gives a 1:1 mixture of meta, para ethyl (4-chloro-1-oxobutyl)benzene acetic acid (119 g). To a slurry of LiOH (23.5 g, 0.56 mol) in water (100 mL) and ethanol (100 mL) is added the 1:1 mixture of meta, para ethyl (4-chloro-1-oxobutyl)benzene acetic acid (50 g, 0.19 mol). The reaction becomes exothermic and is cooled with an ice bath. After 1 hour, the solution is allowed to warm to room temperature. After 18 hours, the mixture is concentrated. Water (400 mL) and conc. HCl are added (until pH 4). Ethyl acetate (600 mL) is added. The organic phase is separated, washed with brine and dried (MgSO4). The solution is heated on a steam bath and charcoal (ca. 3 g) is added. The mixture is filtered through Celite and concentrated. The residue is dissolved in ethyl acetate (300 mL) and heptane (600 mL) with heating. Seed crystals are added. After cooling an organic oil appears. Heptane (500 mL) is added and the mixture is heated to reflux, treated with charcoal (ca. 5 g), filtered and seeded. A solid forms and is collected. 1H NMR shows ca. 4:1 mixture of para:meta isomers. Recrystallization from ethyl acetate/heptane gives 4 (cyclopropylcarbonyl)benzeneacetic acid (4.3 g, 11%).