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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 5-(4-Nitro-[1,2,3]triazol-2-ylmethyl)-furan-2-carboxylic acid methyl ester | HCID 67365326 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)furan-2-yl)methanol | HCID 67365277 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08536209B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-ddf7d1f4a64941a98ee522d46029ed5f |
|---|
| Source note | uspto-grants-2013_09 |
|---|