HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794697Generated: October 25, 2026
Diethoxymethane → ethyl 2-(ethoxymethyl)-5-(4,5-dimethoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate
https://huagongshe.com/reaction/1794697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethoxymethane | HCID 10024 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 178470514 | HCID 178470514 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-(ethoxymethyl)-5-(4,5-dimethoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate | HCID 22222622 | 99% |
Reaction Steps
Ethyl 5-(4,5-dimethoxy-2-nitrobenzoyl)-1H-1,2,3-triazole-4-carboxylate (Synthesis Example 2) (210 mg) and p-toluenesulfonic acid monohydrate (62 mg) were suspended in methylene chloride (5 ml) under an argon atmosphere. Diethoxymethane (0.5 ml) was added to the suspension. The mixture was stirred at 80° C. for 2 hr. The mixture was post-treated by a conventional method and subjected to separation and purification to give ethyl 2-(ethoxymethyl)-5-(4,5-dimethoxy-2-nitrobenzoyl)-2H-1,2,3-triazole-4-carboxylate (242 mg, 99%) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07022860B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-8fa1a6617b5b4d15b92330c562213399 |
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| Source note | uspto-grants-2006_04 |
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