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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42868Generated: October 29, 2026

Nitrogen → 2-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-oxazol-4-ylmethyl]-4-nitro-2H-[1,2,3]triazole

https://huagongshe.com/reaction/42868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-nitro-2H-1,2,3-triazoleHCID 278150—
ReactantHCID 131730013HCID 131730013—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-[2-(tert-Butyl-dimethyl-silanyloxymethyl)-oxazol-4-ylmethyl]-4-nitro-2H-[1,2,3]triazoleHCID 131730849—

Reaction Conditions

Temperature50 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 2-(tert-butyl-dimethyl-silanyloxymethyl)-oxazol-4-ylmethyl ester (651 mg, 2.02 mmol) in DMF (3.0 mL) was added to a solution of 4-nitro-2H-[1,2,3]triazole (210 mg, 1.84 mmol) in DMF (3.0 mL) pre-treated for 30 min with DIPEA (0.63 mL, 3.68 mmol) and the reaction mixture was stirred for 20 h at 50° C. Water (10 mL), followed by EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over NaSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (5:1 to 2:1 hept-EA) gave the title compound as a yellow oil: TLC:rf (1:2 hept-EA)=0.30. LC-MS-conditions 02: tR=1.10 min; [M+H]+=340.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536209B2
Source datasetuspto-grants-2013_09
ORD IDord-9dd3d9f1d6564d0f841f83274e3f2ee8
Source noteuspto-grants-2013_09