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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 645492Erstellt: 25. Oktober 2026

Morpholine → (2-Morpholin-4-yl-2-oxo-1-phenylethyl)carbamic acid tert-butyl ester

https://huagongshe.com/reaction/645492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
Edukt2-(((Tert-butoxy)carbonyl)amino)-2-phenylacetic acidHCID 571805—
EduktEDCl H2OHCID 87672115—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2-Morpholin-4-yl-2-oxo-1-phenylethyl)carbamic acid tert-butyl esterHCID 68708152—

Reaktionsschritte

To a solution of tert-butoxycarbonylaminophenylacetic acid (4.0 mmol) in CH2Cl2 (8.0 mL) is added morpholine (4.0 mmol), EDCl—H2O (4.8 mmol) and DMAP (0.40 mmol) at room temperature. After stirring at room temperature for 24 h, the reaction is quenched by the addition of water. The mixture is extracted with AcOEt. The combined organic extracts are washed with brine, dried over Na2SO4 and concentrated in vacuo. The resulting solid is triturated with ether-n-hexane to give the title compound; 1H NMR (CDCl3) δ 1.41 (s, 9H), 3.08-3.12 (m, 1H), 3.20-3.28 (m, 1H), 3.39-3.45 (m, 1H), 3.49-3.60 (m, 3H), 3.66-3.76 (m, 2H), 5.54 (d, 1H), 6.01 (d, 1H), 7.29-7.36 (m, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07704996B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-a82ea35a0aca46be9699086903d53452
Quellennotizuspto-grants-2010_04