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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352140Erstellt: 24. Oktober 2026

4-Methylmorpholine → 1,1-Dimethylethyl [4-(methoxymethylamino)-4-oxobutyl]-carbamate

https://huagongshe.com/de/reaction/352140

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Edukt4-(((Tert-butoxy)carbonyl)amino)butanoic acidHCID 294894—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,1-Dimethylethyl [4-(methoxymethylamino)-4-oxobutyl]-carbamateHCID 8715177983%

Reaktionsschritte

4-(Dimethylamino)pyridine (6.11 g), N,O-dimethylhydroxylamine hydrochloride(4.88 g), N-methylmorpholine (5.06 g) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (9.58 g) were added in quick succession to a solution of 4-(tert-butoxycarbonylamino)butyric acid (10.16 g) in dichloromethane (200 ml). The reaction mixture was then stirred under ambient conditions for 18 h. The solution was then washed with 2M hydrochloric acid solution, 10% sodium bicarbonate solution and brine. The organic layer was separated, dried over magnesium sulfate, filtered and the filtrate evaporated to dryness to give the subtitle compound as a colourless oil (10.2 g, 83%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743939B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-170e38e4aac64852af941fe35fecce62
Quellennotizuspto-grants-2004_06