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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189363Generated: November 1, 2026

Nitrogen → 2-[4-(2-Methyl-[1,3]dioxolan-2-yl)-butyl]-oxazole-4-carbonyl azide

https://huagongshe.com/reaction/1189363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium AzideHCID 33557—
Reactant2-[4-(2-Methyl-[1,3]dioxolan-2-yl)-butyl]-oxazole-4-carbonyl chlorideHCID 86664901—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-[4-(2-Methyl-[1,3]dioxolan-2-yl)-butyl]-oxazole-4-carbonyl azideHCID 86664902—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), this crude 2-[4-(2-methyl-[1,3]dioxolan-2-yl)-butyl]-oxazole-4-carbonyl chloride was dissolved in acetone (18.0 mL). The solution was cooled to 0° C. and a solution of sodium azide (314 mg, 4.79 mmol) in H2O (2.0 mL) was added over 1 h. The reaction mixture was stirred at 0° C. for 1.5 h then at rt for 45 min. The mixture was concentrated under reduced pressure (coevaporation with toluene) then dissolved in CH2Cl2 and filtered. The filtrate was concentrated under reduced pressure to give the title compound as a yellow oil. LC-MS-conditions 02: tR=0.89 min [M+H]+=281.38.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-c48c2791002d4baea38495ae960b57fb
Source noteuspto-grants-2014_03