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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23684Erstellt: 25. Oktober 2026

N,N,N',N'-Tetramethylethylenediamine → Tert-butyl 2-{4-[(dimethylamino)methyl]phenyl}-2-hydroxyethyl(methyl)carbamate

https://huagongshe.com/reaction/23684

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktAmmonium ChlorideHCID 25517—
Edukt4-DimethylaminomethylbenzaldehydeHCID 193251—
Edukttert-butyl N,N-dimethylcarbamateHCID 312724—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 2-{4-[(dimethylamino)methyl]phenyl}-2-hydroxyethyl(methyl)carbamateHCID 2257434276,3%

Reaktionsschritte

To a solution of tert-butyl dimethylcarbamate (350 mg, 2.4 mmol) and tetramethylethylenediamine (511 mg, 4.4 mmol) in THF (anhydrous, 10 mL) was added sec-butyllithium (1.4 M in cyclohexane, 2.2 mL, 3.1 mmol) at −78° C. The mixture was stirred at that temperature for 1 hour before 4-[(dimethylamino)methyl]benzaldehyde (J.Heterocycl.Chem.; 26; 1989; 1325-1330)(280 mg, 1.7 mmol) was introduced. The reaction mixture was stirred for 2 hours, warmed to room temperature and stirred for 1 hour. Saturated ammonium chloride aqueous solution (10 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 (0.40 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-6511676a45de4e4a8f11cbf1be38cd8d
Quellennotizuspto-grants-2005_02