HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593381Generated: October 25, 2026
Ethyl Acetate → 5-(Azidomethyl)-2-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/1593381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 6-(Trifluoromethyl)nicotinic acid | HCID 2777551 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-(Azidomethyl)-2-(trifluoromethyl)pyridine | HCID 86601757 | 99% |
Reaction Steps
Into ethyl acetate was suspended 1.91 g of 6-(trifluoromethyl)nicotinic acid, and then 1.52 g of triethylamine and 3.03 g of DPPA were added thereto, followed by 3 hours of stirring. The reaction solution was washed with a saturated sodium bicarbonate aqueous solution and saturated saline and the solvent was removed by evaporation to obtain 2.0 g of 6-(trifluoromethyl)nicotinyl azide as a solid. The resulting acid azide was dissolved into 20 ml of toluene and the solution was heated and refluxed to convert the acid azide into 5-isocyanato-2-(trifluoromethyl)pyridine. Thereafter, 1 ml of methanol was added thereto at room temperature, followed by 1 hour of stirring. The reaction solution was washed with water and then dried over anhydrous magnesium sulfate. Thereafter, the solvent was removed by evaporation to obtain 1.2 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07297698B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-39b8ea065d2148aaa6af35237bd0e9f3 |
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| Source note | uspto-grants-2007_11 |
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