Dimethyl Sulfate → Ethyl 4-(2-(tert-butoxycarbonyl(methyl)amino)ethyl)benzoate
Reaktionsgleichung
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][C:11]1[CH:21]=[CH:20][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:22][Si]([N-][Si](C)(C)C)(C)C.[Na+].S(OC)(OC)(=O)=O>C1COCC1>[C:1]([O:5][C:6]([N:8]([CH3:22])[CH2:9][CH2:10][C:11]1[CH:21]=[CH:20][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][CH:12]=1)=[O:7])([CH3:2])([CH3:3])[CH3:4]Komponenten
Reaktionsbedingungen
- Temperatur
- 22 °C
Versuchsvorschrift
To a solution of 1.25 g (4.26 mmol) of ethyl 4-(2-(tert-butoxycarbonylamino)ethyl)benzoate in 40 mL of dry THF under a nitrogen atmosphere was added dropwise, 4.7 mL (4.7 mmol) of NaHMDS (1.0 M in THF) at 0° C. After stirring for 10 min, 0.50 mL (5.3 mmol) of dimethyl sulfate was added and the reaction was warmed to 22° C. and stirred for about 16 h. The reaction was quenched by adding 25 mL of saturated NaHCO3 and the mixture was extracted with DCM (2×25 mL). The combined organic extracts were dried (Na2SO4) and evaporated and the residue was purified by flash chromatography on silica gel, eluting first with hexane and then gradually increasing to 10% ethyl acetate/hexane to give ethyl 4-(2-(tert-butoxycarbonyl(methyl)amino)ethyl)benzoate as a colorless oil.
Aufarbeitung
- customat 0° C
- stirringstirred for about 16 h
- customThe reaction was quenched
- additionby adding 25 mL of saturated NaHCO3
- extractionthe mixture was extracted with DCM (2×25 mL)
- dry with materialThe combined organic extracts were dried (Na2SO4)
- customevaporated
- customthe residue was purified by flash chromatography on silica gel
- washeluting first with hexane
- temperaturegradually increasing to 10% ethyl acetate/hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-6408d5a3ec394cee8bc733ed94daa33e
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09227918B2
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