Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070980Generated: October 31, 2026

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

https://huagongshe.com/reaction/2070980

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 warming 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 3-(azidomethyl)-5-(benzyloxy)pyridine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-0af6e61f1fa9431faeb2d966a2fdee6a
Source noteuspto-grants-2012_10