反応 #40278
ord-be1165b7684041fa91ec2ef11dffc25a
反応方程式
反応物
試薬
反応条件
後処理
- 1その他A 500 mL round bottomed flask equipped with a magnetic stirrer, addition funnel
- 2その他reaction
- 3workup.ADDITIONwas added
- 4workup.STIRRINGwith stirring
- 5その他The organic layer was separated
- 6洗浄washed with 3×100 mL of water
- 7濃縮concentrated at 30° C./60 mmHg to a volume of ca. 60 mL
- 8workup.ADDITIONThe resulting slurry was diluted with 200 mL of heptane
- 9濃縮concentrated at 30° C./60 mmHg to a volume of ca. 150 mL
- 10workup.STIRRINGstirred at 50° C. for 30 min
- 11温度After cooling to room temperature
- 12ろ過the solid was collected by filtration
- 13洗浄washed with 40 mL of 10% ethyl acetate in heptane
- 14その他dried by suction
- 15workup.WAITunder reduced pressure (house vacuum) for 24 h
実験手順
A 500 mL round bottomed flask equipped with a magnetic stirrer, addition funnel, thermocouple probe and nitrogen inlet/outlet was charged with 4.40 mL (76.86 mmol) of acetic acid, 140 mL of DMF and 7.000 g (85.33 mmol) of sodium acetate. Then, 23.30 g (77.62 mmol) of the compound obtained in step 5 was added portionwise over 45 min. After stirring at room temperature for an additional 1 h, HPLC analysis indicated complete reaction. The reaction mixture was diluted with 350 mL of ethyl acetate and 100 mL of saturated sodium bicarbonate was added with stirring. The organic layer was separated, washed with 3×100 mL of water and concentrated at 30° C./60 mmHg to a volume of ca. 60 mL. The resulting slurry was diluted with 200 mL of heptane, concentrated at 30° C./60 mmHg to a volume of ca. 150 mL, and stirred at 50° C. for 30 min. After cooling to room temperature, the solid was collected by filtration, washed with 40 mL of 10% ethyl acetate in heptane and dried by suction, then under reduced pressure (house vacuum) for 24 h, to give 19.52 g (90.0% yield) of the title compound as an off-white solid; 98.81% pure as determined by HPLC analysis (same conditions as in step 4, retention time 6.78 min).