HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257643Generated: October 29, 2026
Tributyltin azide → HCID 178420153, compound
https://huagongshe.com/reaction/257643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin azide | HCID 4984872 | — |
| Reactant | HCID 10022670 | HCID 10022670 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178420153 | HCID 178420153 | 66.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05262540 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-5b76eac683264e43ad5673854d6c0955 |
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| Source note | uspto-grants-1993_11 |
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