HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293120Generated: November 3, 2026
Water → Ethyl 4-(3,4-dimethoxybenzoyl)-1H-1,2,3-triazole-5-carboxylate
https://huagongshe.com/reaction/1293120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Ethyl 4-(3,4-dimethoxyphenyl)-4-oxo-2-butenoate | HCID 53400457 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-(3,4-dimethoxybenzoyl)-1H-1,2,3-triazole-5-carboxylate | HCID 178470512 | 52.9% |
Reaction Steps
A solution (3.0 mL) of ethyl 4-(3,4-dimethoxyphenyl)-4-oxo-2-butenoate (104 mg, 0.39 mmol) in N,N-dimethylformamide was added to a solution (5.0 mL) of sodium azide (40 mg, 0.62 mmol) in N,N-dimethylformamide at 5° C. The temperature of the reaction solution was raised to room temperature before the reaction solution was stirred for 6 hr. After the completion of the reaction, iced water (10 mL) was added to the reaction solution, and the mixture was washed with ethyl acetate. The aqueous layer was then adjusted to pH 1.5 by the addition of 2 N hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was then removed by evaporation under the reduced pressure. The oil thus obtained was dried in vacuo to give ethyl 5-(3,4-dimethoxybenzoyl)-1H-1,2,3-triazole-4-carboxylate (63 mg, yield 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07238719B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-fbb2aec1771c4e0caba76d53e61a8d00 |
|---|
| Source note | uspto-grants-2007_07 |
|---|