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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274681Generated: October 25, 2026

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

https://huagongshe.com/reaction/274681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-3-BromopropylphthalimideHCID 21611—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178418642HCID 178418642—
SolventDimethylformamideHCID 6228—
Product4-(3-Phthalimidopropyloxy)pyridineHCID 1907909016.4%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-2dafe5227f2d4b8c84b36f76fba6ae55
Source noteuspto-grants-1995_02