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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1533470Erstellt: 25. Oktober 2026

Tetrahydrofuran → 1-N-Propylphthalimido-1H-pyrrole-3,4-dicarboxylate diethyl ester

https://huagongshe.com/reaction/1533470

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktN-3-BromopropylphthalimideHCID 21611—
EduktSodium hydrideHCID 24758—
EduktDiethyl 3,4-pyrroledicarboxylateHCID 688199—
Produkt1-N-Propylphthalimido-1H-pyrrole-3,4-dicarboxylate diethyl esterHCID 6973483092%

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

A solution of diethyl pyrrole-3,4-dicarboxylate (39 g, 0.185 mol) in THF (1600 mL) was treated with NaH (60%, 7.6 g, 0.19 mol). The reaction mixture was heated to reflux for 1 hour. The reaction was then cooled to 30° C. and N-(3-bromopropyl)phthalimide (52 g, 0.19 mol) was added. The reaction mixture was heated to reflux for 1 hour, cooled, filtered, and concentrated in vacuo. The resultant gum was partitioned between ETOAC/H2O and extracted with EtOAC (2×300 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The resultant solid was recrystallized from EtOAC to give the title compound 68 g (92%) (mp 100-101° C.). 1H NMR (DMSO) δ1.24 (t, 3H, CH), 2.06 (m, 2H, CH3), 3.57 (t, 2H, CH2), 4.14 (m, 4H, CH2), 7.49 (s, 2H, ArH), 7.86 (m, 4H, ArH)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06207826B1
Quelldatensatzuspto-grants-2001_03
ORD IDord-ebe3117eea7b4e998a60ba06d33a7e04
Quellennotizuspto-grants-2001_03