HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278728Generated: October 25, 2026
Toluene → 5-(Azidomethyl)-2-methylpyrimidine
https://huagongshe.com/reaction/2278728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Diphenylphosphoryl azide | HCID 123414 | — |
| Reactant | (2-Methylpyrimidin-5-yl)methanol | HCID 14686706 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Azidomethyl)-2-methylpyrimidine | HCID 54595022 | — |
Reaction Steps
A solution of (2-methylpyrimidin-5-yl)methanol (0.82 g, 6.6 mmol) in toluene (30 mL, 300 mmol) and methylene chloride (40 mL, 600 mmol) at 0° C. was treated with diphenylphosphonic azide (2.8 mL, 13 mmol) followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (2.0 mL, 13 mmol) and stirred for 2 h at 0° C. After being further stirred at rt for 16 h, the reaction mixture was diluted with water (50 mL) and DCM (50 mL). The organic layer was separated and washed with brine, dried (Mg2SO4), filtered, and concentration. The residue was purified by column to give the product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133122B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-dc6dc165eeaa4449bbfc8b23cb514a24 |
|---|
| Source note | uspto-grants-2015_09 |
|---|