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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608959Generated: November 1, 2026

Sodium Azide → HCID 15220953, compound

https://huagongshe.com/reaction/1608959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(Benzyloxy)benzoic acidHCID 73880—
Reactant4,5-diphenyltetrahydro-3h-pyrazol-3-oneHCID 270492—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 15220953HCID 1522095352%

Reaction Steps

4-Benzyloxybenzoic acid (2.0 g, 8.8 mmol was suspended in 50 mL toluene with oxalyl chloride (5 mL) and heated to reflux for 15 min. Solvent was removed in vacuo, the residue redissolved in 30 mL acetone, and an aqueous solution of NaN3 (1.16 g, 17.6 mmol, 2.0 eq. in 10 mL H2O) added dropwise with external cooling by a water bath. The mixture was stirred for 1 hour, diluted with H2O, extracted twice with toluene, then the combined extracts washed with water and brine, and dried over Na2SO4. This solution of acyl azide was treated with 4,5-diphenyl-3-pyrazolidinone (1.6 g, 6.8 mmol, 0.76 eq.), warmed until bubbles evolved, and heating maintained for 30 min. After stirring overnight at room temperature, the solvent was removed in vacuo, and the product isolated by chromatography (0-30% EtOAc:hexane gradient) as 1.6 g (52%) white solid: mp 127°-30° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399565
Source datasetuspto-grants-1995_03
ORD IDord-41f9d838e63142f4b15332234043c424
Source noteuspto-grants-1995_03