تفاعل #2254221
ord-1d56097024de4e43ab101c80a5960fea
معادلة التفاعل
الكواشف
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المعالجة
- 1درجة الحرارةwas heated
- 2درجة الحرارةat reflux in a 250 ml round bottom flask
- 3أخرىequipped with a Dean-Stark and a reflux condenser
- 4درجة الحرارةAfter cooling
- 5أخرىthe layer was separated
- 6غسيلthe organic was washed by water (120 ml)
- 7استخلاصthe aqueous layer was extracted by CH2Cl2 (3×120 ml)
- 8غسيلThe combined organic was washed with sat'd NaHCO3, brine
- 9أخرىdried
- 10تركيزconcentrated
- 11أخرىthe residual was purified by flash chromatography (340 g silica gel column, eluted by EtOAc in hexane: 5% EtOAc, 2 CV; 5-25%, 14 CV; 25-40%, 8 CV)
- 12أخرىgave
- 13workup.ADDITIONa mixture of E and Z isomers
الإجراء التجريبي
A mixture of 6-oxaspiro[4.5]decan-9-one (13.74 g, 89.1 mmol), methylcyanoacetate (9.4 ml, 106.9 mmol), ammonium acetate (1.79 g, 26.17 mmol) and acetic acid (1.02 ml, 17.8 mmol) in benzene (75 ml) was heated at reflux in a 250 ml round bottom flask equipped with a Dean-Stark and a reflux condenser. After 3 h, TLC (25% EtOAc in hexane, PMA stain) showed the reaction was completed. After cooling, benzene (50 ml) was added and the layer was separated, the organic was washed by water (120 ml) and the aqueous layer was extracted by CH2Cl2 (3×120 ml). The combined organic was washed with sat'd NaHCO3, brine, dried and concentrated and the residual was purified by flash chromatography (340 g silica gel column, eluted by EtOAc in hexane: 5% EtOAc, 2 CV; 5-25%, 14 CV; 25-40%, 8 CV) gave a mixture of E and Z isomers: methyl 2-cyano-2-[6-oxaspiro[4.5]decan-9-ylidene]acetate (18.37 g, 87.8% yield, m/z 236.0 [M+H]+ observed) as a clear oil.