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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473620Generated: October 30, 2026

Sodium Azide → HCID 86687688, compound

https://huagongshe.com/reaction/1473620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantOxalyl chlorideHCID 65578—
Reactant1,3-Oxazole-4-carboxylic acidHCID 14281430—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86687688HCID 8668768897%

Reaction Steps

In a 10-mL round bottom flask under N2 were dissolved 4-oxazolecarboxylic acid (500 mg, 4.42 mmol) and oxalyl chloride (1.94 mL, 22.1 mmol) with 2 drop of DMF in 10 mL of DCM. The reaction was stirred at rt for 2 h. The reaction mixture was concentrated under reduced pressure and the material was carried forward crude. Under N2, oxazole-4-carbonyl chloride (crude) was dissolved in 10 mL of acetone and treated at 0° C. with a solution of sodium azide (575 mg, 8.84 mmol) in 1.0 mL of water. After 1 h, the reaction mixture was diluted with AcOEt then neutralized with H2O. The aqueous phase was extracted 3× with AcOEt then the organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude oxazole-4-carbonyl azide (590 mg, 4.27 mmol, 97% yield) was carried forward without further purification into the next step. MS (ESI, positive ion) [M+1]+: 139.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-5824d11c11d74bf1afe1a03a26f713e8
Source noteuspto-grants-2015_04