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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210136Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-(Phthalimidomethyloxy)pyridine

https://huagongshe.com/reaction/2210136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantChloromethylphthalimideHCID 87154—
ReactantHCID 178418642HCID 178418642—
SolventDimethylformamideHCID 6228—
Product4-(Phthalimidomethyloxy)pyridineHCID 1907910521%

Reaction Steps

To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 10.76 g (55 mmol) of N-chloromethylphthalimide in 80 ml of DMF, 8.23 ml (55 mmol) of 1,8-diazabicyclo[5,4,0]-7-undecene was added. The mixture was stirred at room temperature for 2 hours. After the solvent was distilled off, the reaction mixture was poured into water and extracted with ethyl acetate. The precipitate was filtered off. The aqueous layer was further extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 2.67 g of the desired compound (yield: 21%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-cef321e7bde94b67bdde9d074283ca0e
Source noteuspto-grants-1995_10