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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602130Erstellt: 27. Oktober 2026

Phthalimide → tert-Butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/602130

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalimideHCID 6809—
EduktTriphenylphosphineHCID 11776—
Edukttert-Butyl 2-(hydroxymethyl)morpholine-4-carboxylateHCID 5201202—
EduktDiethylazodicarboxylate tolueneHCID 66777355—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl 2-((1,3-dioxoisoindolin-2-yl)methyl)morpholine-4-carboxylateHCID 5899266097%

Reaktionsschritte

Triphenylphosphine (506 mg, 1.87 mmol) and phthalimide (275 mg, 1.87 mmol) were added to 4-(tert-butoxycarbonyl)morpholin-2-yl methanol (340 mg, 1.56 mmol) in tetrahydrofuran (3 mL). The mixture was stirred at room temperature for 5 min, followed by addition of a 40% diethyl azodicarboxylate/toluene solution (1.06 mL, 2.34 mmol) and stirring at room temperature for 4 hours. Subsequently, ethyl acetate was added and the mixture washed sequentially with tap water and brine. The mixture was then dried over magnesium sulfate and the solvent was evaporated. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=10:1->3:1) gave 524 mg (97%) of the desired compound as a colorless powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902367B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-68037ced14ef487da4480e0c343604ce
Quellennotizuspto-grants-2011_03