HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396284Generated: October 29, 2026
Triethylamine → 5-(azidocarbonyl)-1-phenyl-1H-1,2,3-triazole
https://huagongshe.com/reaction/396284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-Phenyl-1H-1,2,3-triazole-5-carboxylic acid | HCID 2801750 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(azidocarbonyl)-1-phenyl-1H-1,2,3-triazole | HCID 23003629 | 18% |
Reaction Steps
To a solution of 1-phenyl-1H-1,2,3-triazole-5-carboxylic acid (500 mg, 2.64 mmol) in a mixture of acetone (10 mL) and water (5 mL) was added triethylamine (0.55 mL, 3.96 mmol). The mixture was cooled to 0° C. in a ice-bath. Ethylchloroformate (573 mg, 5.28 mmol) was then added and the resulting mixture was stirred for 1.5 hours at 0° C. To the mixture was added sodium azide (0.844 g, 13.0 mmol), and the mixture was stirred for another 1.5 hours. The mixture was concentrated, the residue was diluted with dichloromethane and washed with water. The organic layer was dried over MgSO4 and concentrated to give desired product (100 mg, 18%). 1HNMR (CDCl3) (δ) 8.30 (s, 1H), 7.57 (t, 3H), 7.51 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608077B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-c2dc63dbd1f9482691f9c88b43a0f34d |
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| Source note | uspto-grants-2003_08 |
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