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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42739Generated: October 28, 2026

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

https://huagongshe.com/reaction/42739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium Sodium TartrateHCID 9357—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant5-(4-Nitro-[1,2,3]triazol-2-ylmethyl)-furan-2-carboxylic acid methyl esterHCID 67365326—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(5-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)methanolHCID 67365277—

Reaction Conditions

Temperature-10 °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-[1,2,3]triazol-2-ylmethyl)-furan-2-carboxylic acid methyl ester (325 mg, 1.28 mmol) in THF (13.0 mL) was treated dropwise, at −10° C. with DiBAL (4.36 mL of a 1M solution in toluene, 4.36 mmol). The reaction mixture was stirred at −10° C. for 1 h followed by 1 h at rt. Sat. aq. Rochelle's salt (40 mL) was added and the reaction mixture was stirred for 1 h at rt. The aq. layer was extracted with EA (2×30 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (50:50 hept-EA) gave the title compound: TLC:rf (50:50 hept-EA)=0.28. LC-MS-conditions 02: tR=0.77 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-ddf7d1f4a64941a98ee522d46029ed5f
Source noteuspto-grants-2013_09