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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784923Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 86612599, compound

https://huagongshe.com/reaction/1784923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 57443403HCID 57443403—
SolventTolueneHCID 1140—
ProductHCID 86612599HCID 8661259965%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 250 mg (1.17 mmol) of (5-(benzyloxy)pyridin-3-yl)methanol in 8 mL of toluene was added 310 μL (1.44 mmol) of DPPA. The mixture was cooled to 0° C. and 210 μL (1.44 mmol) of 1,8-diazabicyclo[5.4.0]-undec-7-ene] (DBU) was added. The ice bath was removed, and stirring was continued with wanning to room temperature. After about 20 h, the solution was diluted with EtOAc, and 1N HCl was added to a pH between 7 and 8. The organic layer was washed with water (2×15 mL) and brine (15 mL) and dried over Na2SO4. After filtration and concentration, the crude product was purified by flash silica gel chromatography (56-60% EtOAc/hexanes) to give 181 mg (65% yield) of the azide as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504420B2
Source datasetuspto-grants-2009_03
ORD IDord-0b698925d96c4693929fae997b8485d2
Source noteuspto-grants-2009_03