تفاعل #2719
ord-4ced6f59ef644dca80ccd38e6f9bbbd4
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىwas recooled to -78° C.
- 2workup.STIRRINGThe mixture was stirred for 16 hours at ambient temperature
- 3غسيلwashed with water (10 mL), brine (10 mL)
- 4أخرىdried
- 5أخرىthe solvent was removed by evaporation
- 6أخرىThe product was seperated by column chromatography
- 7workup.DISSOLUTIONwas dissolved in dichloromethane (5 mL)
- 8workup.ADDITIONTo this solution p-TSA (5 mg) was added
- 9workup.STIRRINGthe mixture was stirred at ambient temperature for 5 min
- 10أخرىThe reaction was quenched with 10% NaHCO3 (3 mL)
- 11غسيلwashed with brine (5 mL)
- 12أخرىdried
- 13أخرىthe solvent was removed by distillation
- 14أخرىThe residual crude material was purified by column chromatography
الإجراء التجريبي
To a cold (-78° C.) solution of 2-methylthiophene (1.2 g, 12.2 mmol) in THF (8 mL) was added n-BuLi in hexane (1.6M, 8.5 mL). The mixture was warmed to ambient temperature over 30 minutes. with stirring. The mixture was recooled to -78° C. and a solution of 2,2-dimethyl-6-bromo-thiochroman-4-one (Compound M, 1.4 g, 5.2 mmol) in THF (10 mL) was added. The mixture was stirred for 16 hours at ambient temperature. Then the reaction mixture was diluted with ether (125 mL), washed with water (10 mL), brine (10 mL) dried and the solvent was removed by evaporation. The product was seperated by column chromatography and was dissolved in dichloromethane (5 mL). To this solution p-TSA (5 mg) was added and the mixture was stirred at ambient temperature for 5 min. The reaction was quenched with 10% NaHCO3 (3 mL), washed with brine (5 mL), dried and the solvent was removed by distillation. The residual crude material was purified by column chromatography to obtain the title compound as a pale yellow oil.