反応 #48303
ord-92e11d13934544a5826c16166ebba383
反応方程式
反応物
試薬
反応条件
後処理
- 1workup.ADDITIONwas added
- 2温度at 0° C. and then warmed to RT
- 3その他quenched with saturated ammonium chloride
- 4workup.ADDITIONdiluted with EtOAc and water
- 5その他The layers were separated
- 6抽出the aqueous layer was extracted with EtOAc
- 7洗浄The combined organic layers were washed with a 9:1 aqueous solution of saturated ammonium chloride/ammonium hydroxide, water, brine
- 8乾燥dried over sodium sulfate
- 9workup.DISSOLUTIONThe crude product was dissolved in isopropylacetate (4 mL)
- 10workup.ADDITIONwas added
- 11温度After 30 minutes the reaction was cooled
- 12洗浄washed twice with saturated sodium bicarbonate, once with water, brine
- 13乾燥dried over sodium sulfate
- 14濃縮concentrated
実験手順
(4S,5S)-Tert-butyl 5-((tert-butyldimethylsilyloxy)methyl)-2,2-dimethyl-4-(pyridin-4-ylmethyl)oxazolidine-3-carboxylate (0.150 g, 0.344 mmol) was dissolved in THF (3.5 mL) and cooled to 0° C. Acetyl chloride (0.0256 ml, 0.361 mmol) was added and the reaction was stirred 30 minutes before METHYLMAGNESIUM BROMIDE (0.294 ml, 0.412 mmol) was added. The reaction was stirred 1 hr. at 0° C. and then warmed to RT and quenched with saturated ammonium chloride and diluted with EtOAc and water. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with a 9:1 aqueous solution of saturated ammonium chloride/ammonium hydroxide, water, brine, and dried over sodium sulfate. The crude product was dissolved in isopropylacetate (4 mL) and heated to 50° C. before DDQ (0.117 g, 0.515 mmol) was added. After 30 minutes the reaction was cooled and diluted with ethyl acetate and washed twice with saturated sodium bicarbonate, once with water, brine, and dried over sodium sulfate. The mixture was passed through a plug of silica gel with 2:1 Hexanes/EtOAc and concentrated to afford the title compound, MS m/z: 451.3(100%, M+1)).