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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293116Generated: November 1, 2026

Water → Ethyl 4-(3,4-dimethoxybenzoyl)-1H-1,2,3-triazole-5-carboxylate

https://huagongshe.com/reaction/1293116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AzideHCID 33557—
ReactantEthyl 4-(3,4-dimethoxyphenyl)-4-oxo-2-butenoateHCID 53400457—
CatalystCuprous chlorideHCID 62652—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(3,4-dimethoxybenzoyl)-1H-1,2,3-triazole-5-carboxylateHCID 17847051265%

Reaction Steps

Copper(I) chloride (7.5 mg, 0.075 mmol) was added at room temperature to a solution (1.0 mL) of sodium azide (74 mg, 1.1 mmol) in N,N-dimethylformamide. A solution (1.5 mL) of ethyl 4-(3,4-dimethoxyphenyl)-4-oxo-2-butenate (200 mg, 0.76 mmol) in N,N-dimethylformamide was added to this mixed solution at 5° C. The temperature of the reaction solution was raised to room temperature before the reaction solution was stirred for 8 hr. After the completion of the reaction, the reaction solution was poured into iced water, and the mixture was extracted with a saturated aqueous sodium hydrogencarbonate solution. The aqueous layer was adjusted to pH 1.8 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 (149 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238719B2
Source datasetuspto-grants-2007_07
ORD IDord-9889bb24b6c64e219c87b525d58cb7ed
Source noteuspto-grants-2007_07