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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82801Generated: October 26, 2026

Nitrogen → 2-((5-(methoxymethyl)furan-2-yl)methyl)-4-nitro-2H-1,2,3-triazole

https://huagongshe.com/reaction/82801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantMethyl iodideHCID 6328—
Reactant(5-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)methanolHCID 67365277—
SolventDichloromethaneHCID 6344—
Product2-((5-(methoxymethyl)furan-2-yl)methyl)-4-nitro-2H-1,2,3-triazoleHCID 67958035—

Reaction Conditions

Temperature40 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (5-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)methanol (WO 2009077990A1) (186 mg, 0.83 mmol) in CH2Cl2 (3.0 mL) was added to a suspension of Ag2O (288 mg, 1.24 mmol) and MeI (0.06 mL, 0.99 mmol). The resulting mixture (protected form light) was stirred overnight at 40° C. The reaction mixture was filtered and the solvent was removed under reduced pressure. Purification of the residue by FC (7:3 hept-EA) gave the title compound as a yellow oil: TLC: rf (7:3 hept-EA)=0.27. LC-MS-conditions 07: tR=0.74 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846733B2
Source datasetuspto-grants-2014_09
ORD IDord-569616292ed94a7bbabf1c84837cc584
Source noteuspto-grants-2014_09