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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2736Erstellt: 23. Oktober 2026

Morpholine → Morpholino(3-nitrophenyl)methanone

https://huagongshe.com/de/reaction/2736

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
Edukt3-Nitrobenzoic acidHCID 8497—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMorpholino(3-nitrophenyl)methanoneHCID 22545389,8%

Reaktionsschritte

In tetrahydrofuran (100 ml) and dichloromethane (100 ml), 3-nitrobenzoic acid (7.58 g) was dissolved. Then 1-hydroxybenzotriazole (6.74 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (9.57 g), and morpholine (9.47 g) were added to the solution. The mixture was stirred at room temperature overnight. After the reaction was completed, chloroform was added to the solution. The mixture was washed with 1N-HCl aqueous solution, 1N-NaOH aqueous solution, and distilled water. The organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (Kieselgel 60=160 g, ethyl acetate) to obtain the above-captioned compound ([13]-(132)-158) (9.62 g) as white crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05731310
Quelldatensatzuspto-grants-1998_03
ORD IDord-92408f87220947e8aa462aa1b48b9d43
Quellennotizuspto-grants-1998_03