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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6138Erstellt: 24. Oktober 2026

N-3-Bromopropylphthalimide → 4-(3-Phthalimidopropyloxy)pyridine

https://huagongshe.com/de/reaction/6138

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-3-BromopropylphthalimideHCID 21611—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktHCID 178418642HCID 178418642—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(3-Phthalimidopropyloxy)pyridineHCID 1907909016,4%

Reaktionsschritte

To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 14.75 g (55 mmol) of N-(3-bromopropyl)phthalimide in 80 ml of DMF was added 8.23 ml (55 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene. The mixture was stirred at room temperature for 6 hours. After the solvent was distilled off, the mixture was poured into water and extracted with ethyl acetate. The mixture was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 2.32 g of the desired compound (yield: 16.4%, colorless crystals).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246948
Quelldatensatzuspto-grants-1993_09
ORD IDord-9416feec1e0e4637adb9bb2ca9dd4492
Quellennotizuspto-grants-1993_09