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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30314Erstellt: 24. Oktober 2026

Dimethylformamide → N-benzyl-2-(morpholin-4-carbonyl)-morpholine hydrochloride

https://huagongshe.com/de/reaction/30314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktMorpholineHCID 8083—
EduktOxalyl chlorideHCID 65578—
Edukt4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 2776352—
Lösungsmittel1,1-DichloroethaneHCID 6365—
ProduktN-benzyl-2-(morpholin-4-carbonyl)-morpholine hydrochlorideHCID 68436268—

Reaktionsbedingungen

Temperatur62.5 °C

Reaktionsschritte

A 250 mL reactor under N2 is successively loaded with 91 (5 g, 19.41 mmol), dichloroethane (50 mL), DMF (0.014 mL, 1% mol) and oxalyl chloride (1.86 mL, 21.35 mmol). The mixture is heated up to 60-65° C. for 2 h, before being cooled to 0° C. Then, morpholine (6.93 g, 79.60 mmol) in dichloroethane (20 mL) is added over 15 min keeping the temperature below 10° C. The heterogeneous solution is post-agitated for 1 h 30 min at room temperature and quenched with water (30 mL). The biphasic mixture is filtered on a Hyflo Super Cel® (10 g), then after separation, the organic layer is concentrated under reduce pressure. The mixture is taken up with isopropanol (80 mL) and 12N HClaq (1.61 mL, 19.41 mmol), stirred for 10 min and concentrated under reduce pressure. The mixture is taken up with isopropanol (13 mL), heated to reflux until a homogeneous solution is formed, then it is cooled to room temperature. The precipitate is filtered, rinsed with isopropanol (10 mL) and dried under vacuum at 40° C. overnight to obtain 92 as an off-white powder with 79% overall yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423037B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-427226a221e043c0b74882f62f2c6aba
Quellennotizuspto-grants-2008_09