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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1365125Erstellt: 26. Oktober 2026

N,N,N',N'-Tetramethylethylenediamine → Methyl 3-((tert-butoxycarbonyl)amino)furan-2-carboxylate

https://huagongshe.com/reaction/1365125

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktDimethyl CarbonateHCID 12021—
Edukttert-butyl N-(furan-3-yl)carbamateHCID 12207186—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-((tert-butoxycarbonyl)amino)furan-2-carboxylateHCID 5298767051%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of tert-butyl furan-3-ylcarbamate 32 (1.7 g, 1.0 eq) in THF (50 ml) at −30° C. was added TMEDA (1.75 ml, 1.3 eq) followed by 1.6M solution of n-butyllithium (8.4 ml, 2.25 eq, 1.6M in hexanes). Reaction mixture was allowed to warm up to 0° C. and stirred for 1 h, before being cooled back to −30° C. Dimethyl carbonate (2.4 ml, 3.0 eq) was quickly added, before the reaction mixture was allowed to warm up to room temperature for 1 hr. Reaction mixture was quenched with 2M HCl, followed by addition of saturated aq. NaCl. Mixture was extracted with ethyl acetate. The combined organic extracts were dried with Na2SO4 and concentrated. The crude reaction mixture was purified by flash chromatography to yield tert-butyl 2-(methoxycarbonyl)furan-3-ylcarbamate 33 (1.14 g, 51%): MS (Q1) 242 (M)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07888352B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-a0bf178147f146f18554b3de636500d4
Quellennotizuspto-grants-2011_02