تفاعل #81616
ord-f7758f879e18489a8a13adc08d5ddac0
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةPlace under a nitrogen atmosphere, cool to 0°-5° C.
- 2أخرىat approximately 0° C
- 3أخرىquench
- 4workup.ADDITIONby slowly pouring over approximately 2L of crushed ice
- 5workup.STIRRINGAdd methylene chloride (500 mL) and stir for 5 minutes
- 6أخرىSeparate the organic phase
- 7استخلاصextract the aqueous phase with methylene chloride (300 mL)
- 8غسيلCombine the organic phases and wash with saturated aqueous sodium hydrogen carbonate (3×200 mL), with deionized water (200 mL) and brine (200 mL)
- 9تجفيفDry (MgSO4)
- 10workup.STIRRINGstir for 30 minutes
- 11ترشيحbefore filtering
- 12أخرىEvaporate the solvent in vacuo
- 13أخرىpurify by chromatography (ethyl acetate/hexane)
الإجراء التجريبي
Charge a flask with aluminum chloride (223 g, 1.68 mol) and methylene chloride (200 mL). Place under a nitrogen atmosphere, cool to 0°-5° C. and add, by dropwise addition, ω-chlorobutyryl chloride (188.6 g, 1.34 mol). After acid chloride addition is complete, add, by dropwise addition, 2,2-dimethylphenethyl acetate (128.0 g, 0.67 mol ), keeping the temperature at approximately 0° C. Continue stirring at 0° C. for 2 hours, quench by slowly pouring over approximately 2L of crushed ice. Add methylene chloride (500 mL) and stir for 5 minutes. Separate the organic phase and extract the aqueous phase with methylene chloride (300 mL). Combine the organic phases and wash with saturated aqueous sodium hydrogen carbonate (3×200 mL), with deionized water (200 mL) and brine (200 mL). Dry (MgSO4) and stir for 30 minutes before filtering. Evaporate the solvent in vacuo and purify by chromatography (ethyl acetate/hexane) to give the title compound as an orange/brown oil.