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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 530772Erstellt: 27. Oktober 2026

Phthalimide → (S)-(+)-N-(2,3-Epoxypropyl)phthalimide

https://huagongshe.com/reaction/530772

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalimideHCID 6809—
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Edukt(-)-GlycidolHCID 6973630—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S)-(+)-N-(2,3-Epoxypropyl)phthalimideHCID 71941273,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a cold solution of (S)-1-oxiranylmethanol (5 g, 67.5 mmol) and phthalimide (9.9 g, 67.3 mmol) in tetrahydrofuran (200 mL) in ice bath was added triphenylphosphine (17.9 g, 68.2 mmol) and diethyl azodicarboxylate (12.3 g, 70.6 mmol). The mixture was stirred at 0° C. for 2 h and at ambient temperature for 48 h. The mixture was concentrated under vacuum, and the oily residue was purified by flash silica column chromatography, yielding the desired product (10.1 g) as pale yellow solid: Rf=0.51 in 1:1 EtOAc/hexane. 1H-NMR (CDCl3, 300 MHz): δ (ppm) 7.76-7.64 (m, 2H), 7.63-7.60 (m, 2H), 3.9-3.8 (dd, 1H), 3.70-3.65 (dd, 1H), 3.15 (m, 1H), 2.70-2.67 (dd, 1H), 2.58-2.55 (dd, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09353106B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-59351a671ac5486fb6151b450be85875
Quellennotizuspto-grants-2016_05