تفاعل #50878
ord-6a7ee6954ddc497abbbbcc193478656f
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةcooled to 0°
- 2workup.STIRRINGThe reaction was stirred 2 hours at room temperature
- 3workup.ADDITIONwas added
- 4استخلاصThe mixture was extracted with ethyl acetate, which
- 5تجفيفwas dried over sodium sulfate
- 6أخرىevaporated
- 7أخرىPurification of the residue by flash chromatography
الإجراء التجريبي
To a suspension of diacid (Example 25) (0.3 g) in dichloromethane (20 mL), acetonitrile (5 mL) and triethylamine (200 μL) was added 2-chloro-1-methylpyridinium iodide (180 mg). The mixture was stirred 30 min, cooled to 0° and 0.32 mL of a 2M solution of dimethylamine in toluene was added. The reaction was stirred 2 hours at room temperature. The reaction mixture was poured onto NH4OAc buffer and acetic acid (5 mL) was added. The mixture was extracted with ethyl acetate, which was dried over sodium sulfate and evaporated. Purification of the residue by flash chromatography starting with 15% and finishing with 30% of THF in toluene containing 1% of acetic acid afforded the title compound.