반응 #48303
ord-92e11d13934544a5826c16166ebba383
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시약
반응 조건
후처리
- 1workup.ADDITIONwas added
- 2온도at 0° C. and then warmed to RT
- 3기타quenched with saturated ammonium chloride
- 4workup.ADDITIONdiluted with EtOAc and water
- 5기타The layers were separated
- 6추출the aqueous layer was extracted with EtOAc
- 7세척The combined organic layers were washed with a 9:1 aqueous solution of saturated ammonium chloride/ammonium hydroxide, water, brine
- 8건조dried over sodium sulfate
- 9workup.DISSOLUTIONThe crude product was dissolved in isopropylacetate (4 mL)
- 10workup.ADDITIONwas added
- 11온도After 30 minutes the reaction was cooled
- 12세척washed twice with saturated sodium bicarbonate, once with water, brine
- 13건조dried over sodium sulfate
- 14농축concentrated
실험 절차
(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)).