Reaktion #51751
ord-be050adf2f374660821e0dfc54325ed2
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONAfter the addition
- 2workup.STIRRINGthe solution was stirred at −35° C. for 30 minutes
- 3TemperaturThe reaction mixture was slowly warmed to room temperature
- 4Sonstigewas quenched with saturated NH4Cl solution
- 5workup.ADDITIONEtOAc (200 mL) was added
- 6Waschenthe organic layer was washed with brine
- 7Trocknendried (MgSO4)
- 8Einengenconcentrated
- 9workup.DISSOLUTIONThe residue was dissolved in 100 mL of THF
- 10workup.STIRRING2 mL of concentrated HCl and stirred at room temperature for 1 hour
- 11workup.ADDITIONThe solution was diluted with EtOAc
- 12Waschenwashed with NaHCO3 solution and brine
- 13Trocknendried (MgSO4)
- 14SonstigeThe crude product was purified by flash silica gel chromatography
Vorschrift
(5-tert-Butyl-4-mercapto-2-methyl-phenyl)-carbamic acid tert-butyl ester (prepared in Example EE; 20 g, 68 mmol) was dissolved in 100 mL of THF, cooled to −40° C., and treated dropwise with sec-butyllithium (1.3 M, 156 mL, 203 mmol). After the addition was complete, the reaction mixture was stirred at −30° C. to −45° C. for 30 minutes. To the mixture was added DMF (14.8 g, 203.39 mmol), and the solution was stirred at −35° C. for 30 minutes. The reaction mixture was slowly warmed to room temperature and was quenched with saturated NH4Cl solution. EtOAc (200 mL) was added; the organic layer was washed with brine, dried (MgSO4) and concentrated. The residue was dissolved in 100 mL of THF and 2 mL of concentrated HCl and stirred at room temperature for 1 hour. The solution was diluted with EtOAc, washed with NaHCO3 solution and brine, and dried (MgSO4). The crude product was purified by flash silica gel chromatography to give the title compound. MS(APCI): 304 (M−H).