تفاعل #81616

ord-f7758f879e18489a8a13adc08d5ddac0

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةPlace under a nitrogen atmosphere, cool to 0°-5° C.
  2. 2
    أخرىat approximately 0° C
  3. 3
    أخرىquench
  4. 4
    workup.ADDITIONby slowly pouring over approximately 2L of crushed ice
  5. 5
    workup.STIRRINGAdd methylene chloride (500 mL) and stir for 5 minutes
  6. 6
    أخرىSeparate the organic phase
  7. 7
    استخلاصextract the aqueous phase with methylene chloride (300 mL)
  8. 8
    غسيلCombine the organic phases and wash with saturated aqueous sodium hydrogen carbonate (3×200 mL), with deionized water (200 mL) and brine (200 mL)
  9. 9
    تجفيفDry (MgSO4)
  10. 10
    workup.STIRRINGstir for 30 minutes
  11. 11
    ترشيحbefore filtering
  12. 12
    أخرىEvaporate the solvent in vacuo
  13. 13
    أخرىpurify 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05618940uspto-grants-1997_04