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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278728Generated: October 25, 2026

Toluene → 5-(Azidomethyl)-2-methylpyrimidine

https://huagongshe.com/reaction/2278728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiphenylphosphoryl azideHCID 123414—
Reactant(2-Methylpyrimidin-5-yl)methanolHCID 14686706—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(Azidomethyl)-2-methylpyrimidineHCID 54595022—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133122B2
Source datasetuspto-grants-2015_09
ORD IDord-dc6dc165eeaa4449bbfc8b23cb514a24
Source noteuspto-grants-2015_09