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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398350Generated: October 26, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-(Azidomethyl)-1H-1,3-benzodiazole

https://huagongshe.com/reaction/398350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-(Hydroxymethyl)-1H-benzimidazoleHCID 13505556—
SolventTetrahydrofuranHCID 8028—
Product5-(Azidomethyl)-1H-1,3-benzodiazoleHCID 23000173—

Reaction Steps

To a cooled (0° C.) suspension of 5-(hydroxymethyl)-benzimidazole (920 mg, 6.2 mmol) in THF (12 mL) was added sequentially DPPA (1.46 mL, 6.8 mmol) and DBU (1.11 mL, 7.4 mmol). The resulting solution was heated to reflux for 5 h, cooled to RT, and concentrated in vacuo. The residue was partitioned between sodium bicarbonate and ethyl acetate. The organic layer was washed with brine, dried (Na2SO4), and concentrated in vacuo. Silica gel chromatography (15% MeOH—CHCl3), afforded the title compound as a brown solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610692B1
Source datasetuspto-grants-2003_08
ORD IDord-c8af5f06729a4bdfa7640ff663c00ac4
Source noteuspto-grants-2003_08