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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10172Erstellt: 24. Oktober 2026

Phenyl isocyanate → [5-((Morpholin-4-yl)methyl)-4,5-dihydro-isoxazol-3-yl]methyl 2-tetrahydropyranyl ether

https://huagongshe.com/de/reaction/10172

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenyl isocyanateHCID 7672—
EduktTriethylamineHCID 8471—
EduktAllylmorpholineHCID 136522—
Edukt2-(2-Nitroethoxy)tetrahydropyranHCID 3748656—
LösungsmittelTolueneHCID 1140—
Produkt[5-((Morpholin-4-yl)methyl)-4,5-dihydro-isoxazol-3-yl]methyl 2-tetrahydropyranyl etherHCID 2197877144,3%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

To a solution of N-allylmorpholine (0.76 g, 5.0 mmol) in toluene (10 mL) was added 2-(2-nitroethoxy)tetrahydropyran (1.34 g, 7.7 mmol), phenylisocyanate (2:43 g, 20.1 mmol), and triethylamine (52 mg; 0.5 mmol). The resulting mixture was heated at 55° C. overnight. After cooling to room temperature the formed precipitate was removed by filtration and the remaining solution concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH/NH4OH 96/3.75/0.25) to yield 0.63 g (44%) of [5-((morpholin-4-yl)methyl)-4,5-dihydro-isoxazol-3-yl]methyl 2-tetrahydropyranyl ether. MH+ 285, Rf 0.34 (CH2Cl2/MeOH/NH4OH 96/3.75/0.25).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094779B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f898d1d16b634156866bfd923aef5933
Quellennotizuspto-grants-2006_08