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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 57443403 | HCID 57443403 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86612599 | HCID 86612599 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08299267B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-0af6e61f1fa9431faeb2d966a2fdee6a |
|---|
| Source note | uspto-grants-2012_10 |
|---|