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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797110Generated: November 2, 2026

Phthalimide → 2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1797110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactant(6-Bromopyridin-2-yl)methanolHCID 3517811—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
Product2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dioneHCID 2217644666%

Reaction Steps

A solution of (6-bromo-pyridin-2-yl)-methanol (3.37 g, 17.9 mmol) (H. Tsukube et al., J. Org. Chem., 1993, 58, 4389), triphenylphosphine (5.17 g, 19.7 mmol) and phtalimide (2.90 g, 19.7 mmol) in THF was cooled in an ice bath. A solution of diethylazodicarboxylate (3.43 g, 19.7 mmol) in THF (15 ml) was added slowly and the mixture was left to reach rt. Stirring was continued for 17 hr, then the solvent was distilled off and the residue chromatographed (SiO2 with hexane/AcOEt=4/1) to provide 3.42 g (66%) of the title compound as a colorless viscous oil. MS: m/e=316 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034044B2
Source datasetuspto-grants-2006_04
ORD IDord-33ec9cdb62b0456ea0063b451ebce465
Source noteuspto-grants-2006_04