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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257643Generated: October 29, 2026

Tributyltin azide → HCID 178420153, compound

https://huagongshe.com/reaction/257643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin azideHCID 4984872—
ReactantHCID 10022670HCID 10022670—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
ProductHCID 178420153HCID 17842015366.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 2-[3-[2-(4,5-diphenyl-2-oxazolyl)ethyl]phenoxy]acetonitrile (1.60 g, 4.2 mmol) and tri-n-butyltin azide (1.45 g, 4.4 mmol) was stirred at 140° C. under an atomosphere of nitrogen. After 20 hours, the mixture was cooled, diluted with ethyl acetate (300 mL) and 1N HCl (200 mL) and the mixture stirred for 2 hours. The aqueous phase was removed and the organic phase added to 0.1M potassium fluoride solution. After stirring overnight, the organic layer was separated, washed with water and saturated sodium chloride solution, dried over sodium sulfate and concentrated in vacuo. The residue was chromatographed on a column of silica gel using a mixture of chloroform and methanol (10:1) as eluent to give 5-[[3-[2-(4,5-diphenyl-2-oxazolyl)ethyl]phenoxy]methyl]-1H-tetrazole (1.18 g, 66%) after recrystallization from a mixture of hexanes and CH2Cl2 m.p. 138.5°-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262540
Source datasetuspto-grants-1993_11
ORD IDord-5b76eac683264e43ad5673854d6c0955
Source noteuspto-grants-1993_11