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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841971Generated: October 26, 2026

Ethyl ketone → ethyl 5-(4,5-dimethoxy-2-nitrobenzoyl)-2-(3-methoxypentan-3-yl)-2H-1,2,3-triazole-4-carboxylate

https://huagongshe.com/reaction/841971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ketoneHCID 7288—
ReactantTrimethyl orthoformateHCID 9005—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 178470514HCID 178470514—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Productethyl 5-(4,5-dimethoxy-2-nitrobenzoyl)-2-(3-methoxypentan-3-yl)-2H-1,2,3-triazole-4-carboxylateHCID 2222260478%

Reaction Steps

p-Toluenesulfonic acid monohydrate (20 mg) was added to a solution of 3-pentanone (3.1 ml) and trimethyl orthoformate (3.3 ml) in methylene chloride (10 ml). The mixture was heated for one hr with stirring. This solution (4 ml) was added to a solution of ethyl 5-(4,5-dimethoxy-2-nitrobenzoyl)-1H-1,2,3-triazole-4-carboxylate (Synthesis Example 2) (140 mg) in methylene chloride (2 ml). The mixture was stirred at room temperature for one hr, and triethylamine (0.05 ml) was then added thereto. The mixture was post-treated by a conventional method and subjected to separation and purification to give ethyl 5-(4,5-dimethoxy-2-nitrobenzoyl)-2-(3-methoxypentan-3-yl)-2H-1,2,3-triazole-4-carboxylate (140 mg, 78%) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372735B1
Source datasetuspto-grants-2002_04
ORD IDord-a1da1e59376f4493b1f97a6190d14fe6
Source noteuspto-grants-2002_04