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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23688Erstellt: 23. Oktober 2026

N,N,N',N'-Tetramethylethylenediamine → Tert-butyl 2-hydroxy-2-(6-methoxypyridin-3-yl)ethyl(methyl)carbamate

https://huagongshe.com/de/reaction/23688

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktAmmonium ChlorideHCID 25517—
Edukttert-butyl N,N-dimethylcarbamateHCID 312724—
Edukt6-Methoxypyridine-3-carbaldehydeHCID 3364576—
KatalysatorCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 2-hydroxy-2-(6-methoxypyridin-3-yl)ethyl(methyl)carbamateHCID 2257435042,5%

Reaktionsschritte

To a solution of tert-butyl dimethylcarbamate (1.8 g, 0.012 mol) and tetramethylethylenediamine (2.6 g, 0.022 mol) in THF (anhydrous, 30 mL) was added sec-butyllithium (1.4 M in cyclohexane, 11 mL, 0.015 mmol) at −78° C. The mixture was stirred at that temperature for 30 minutes before a solution of 6-methoxy-3-pyridinecarboxaldehyde (J.Org.Chem. 55; 1; 1990; 69-73)(1.4 g, 0.01 mol, in 5 mL of dry THF) was introduced. The reaction mixture was stirred for 30 minutes, warmed to room temperature and stirred for 3 hours. Saturated ammonium chloride aqueous solution (20 mL) was added to quench the reaction after the reaction mixture was cooled to −78° C. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The organic phases were combined, washed with brine and dried over sodium sulfate and concentrated. The residue was purified with a silica gel column to give the title compound (1.2 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-52b78418d3a14c42bc535d0a0cefcfc5
Quellennotizuspto-grants-2005_02