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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274670Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/274670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantChloromethylphthalimideHCID 87154—
ReactantHCID 178418642HCID 178418642—
Solvent1,2-DimethoxyethaneHCID 8071—
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 DME, 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 numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-a5746cad3c7d4189b20bf58111b929bf
Source noteuspto-grants-1995_02