تفاعل #578782
ord-c9673f858bba46509945e5e70e6a597e
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1تركيزThe mixture was concentrated in vacuo
- 2workup.DISSOLUTIONdissolved in Et2O
- 3غسيلwashed once with water
- 4تجفيفThe organic layer was dried over Na2SO4
- 5ترشيحfiltered
- 6تركيزconcentrated in vacuo
- 7workup.ADDITIONThe residue was treated with a mixture of hexanes and EtOAc (1:1)
- 8ترشيحthe solid was filtered
- 9أخرىThe filtrate was evaporated
- 10أخرىthe residue was purified by silica gel column chromatography
الإجراء التجريبي
To a solution of 2-chloro-5-nitro phenol (10 g, 63.497 mmol), N-boc-4-piperidine methanol (13.67 g, 63.49 mmol), and PPh3 (16.63 g, 63.49 mmol) in 130 mL THF, cooled at −20° C. was added dropwise over 1.5 h a 50 mL THF solution containing DIAD (12.75 ml, 64.76 mmol). The mixture turned a deep red. The reaction was warmed gradually to RT and stirred for 18 h. The mixture was concentrated in vacuo, dissolved in Et2O, washed once with water, then NaHCO3 (sat). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was treated with a mixture of hexanes and EtOAc (1:1) and the solid was filtered. The filtrate was evaporated and the residue was purified by silica gel column chromatography to yield the title compound as a yellow solid. MS (MH+)=NA; Calc'd 370.13 for C17H23ClN2O5.